Name: rs35775585
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs35775585

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:9325787-9325802 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₆ / del(A)₅ / del(A)₄ / delA…
del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₆=0.2774 (1389/5008, 1000G)
delA=0.3995 (1722/4310, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF559 : Intron Variant
ZNF559-ZNF177 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	4310	AAAAAAAAAAAAAAAA=0.1580	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.4425, AAAAAAAAAAAAAAA=0.3995, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	0.247664	0.224967	0.52737	3
European	Sub	4302	AAAAAAAAAAAAAAAA=0.1578	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.4428, AAAAAAAAAAAAAAA=0.3993, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	0.248161	0.224749	0.52709	3
African	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	8	AAAAAAAAAAAAAAAA=0.2	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.2, AAAAAAAAAAAAAAA=0.5, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	0.0	0.333333	0.666667	0

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₁₆=0.2774	delAA=0.7226
1000Genomes	African	Sub	1322	(A)₁₆=0.2126	delAA=0.7874
1000Genomes	East Asian	Sub	1008	(A)₁₆=0.2490	delAA=0.7510
1000Genomes	Europe	Sub	1006	(A)₁₆=0.3280	delAA=0.6720
1000Genomes	South Asian	Sub	978	(A)₁₆=0.336	delAA=0.664
1000Genomes	American	Sub	694	(A)₁₆=0.285	delAA=0.715
Allele Frequency Aggregator	Total	Global	4310	(A)₁₆=0.1580	del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.4425, delA=0.3995, dupA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	4302	(A)₁₆=0.1578	del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.4428, delA=0.3993, dupA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	Other	Sub	8	(A)₁₆=0.2	del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.2, delA=0.5, dupA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₁₆=0	del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dup(A)₄=0, dup(A)₅=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₁₆=0	del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dup(A)₄=0, dup(A)₅=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₆=0	del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dup(A)₄=0, dup(A)₅=0
Allele Frequency Aggregator	African	Sub	0	(A)₁₆=0	del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dup(A)₄=0, dup(A)₅=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₆=0	del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dup(A)₄=0, dup(A)₅=0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 19	NC_000019.10:g.9325797_9325802del
GRCh38.p14 chr 19	NC_000019.10:g.9325798_9325802del
GRCh38.p14 chr 19	NC_000019.10:g.9325799_9325802del
GRCh38.p14 chr 19	NC_000019.10:g.9325800_9325802del
GRCh38.p14 chr 19	NC_000019.10:g.9325801_9325802del
GRCh38.p14 chr 19	NC_000019.10:g.9325802del
GRCh38.p14 chr 19	NC_000019.10:g.9325802dup
GRCh38.p14 chr 19	NC_000019.10:g.9325800_9325802dup
GRCh38.p14 chr 19	NC_000019.10:g.9325799_9325802dup
GRCh38.p14 chr 19	NC_000019.10:g.9325798_9325802dup
GRCh38.p14 chr 19	NC_000019.10:g.9325795_9325802dup
GRCh37.p13 chr 19	NC_000019.9:g.9436473_9436478del
GRCh37.p13 chr 19	NC_000019.9:g.9436474_9436478del
GRCh37.p13 chr 19	NC_000019.9:g.9436475_9436478del
GRCh37.p13 chr 19	NC_000019.9:g.9436476_9436478del
GRCh37.p13 chr 19	NC_000019.9:g.9436477_9436478del
GRCh37.p13 chr 19	NC_000019.9:g.9436478del
GRCh37.p13 chr 19	NC_000019.9:g.9436478dup
GRCh37.p13 chr 19	NC_000019.9:g.9436476_9436478dup
GRCh37.p13 chr 19	NC_000019.9:g.9436475_9436478dup
GRCh37.p13 chr 19	NC_000019.9:g.9436474_9436478dup
GRCh37.p13 chr 19	NC_000019.9:g.9436471_9436478dup

Gene: ZNF559-ZNF177, ZNF559-ZNF177 readthrough (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF559-ZNF177 transcript variant 2	NM_001172650.3:c.-480+101… NM_001172650.3:c.-480+1017_-480+1022del	N/A	Intron Variant
ZNF559-ZNF177 transcript variant 4	NM_001202425.1:c.-392+101… NM_001202425.1:c.-392+1017_-392+1022del	N/A	Intron Variant
ZNF559-ZNF177 transcript variant 5	NM_001384659.1:c.-770+101… NM_001384659.1:c.-770+1017_-770+1022del	N/A	Intron Variant

Gene: ZNF559, zinc finger protein 559 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF559 transcript variant 1	NM_001202406.1:c.136+1017… NM_001202406.1:c.136+1017_136+1022del	N/A	Intron Variant
ZNF559 transcript variant 3	NM_001202407.3:c.-193+101… NM_001202407.3:c.-193+1017_-193+1022del	N/A	Intron Variant
ZNF559 transcript variant 4	NM_001202408.1:c.136+1017… NM_001202408.1:c.136+1017_136+1022del	N/A	Intron Variant
ZNF559 transcript variant 5	NM_001202409.2:c.-195+101… NM_001202409.2:c.-195+1017_-195+1022del	N/A	Intron Variant
ZNF559 transcript variant 6	NM_001202410.2:c.-127+101… NM_001202410.2:c.-127+1017_-127+1022del	N/A	Intron Variant
ZNF559 transcript variant 7	NM_001202411.2:c.-156+101… NM_001202411.2:c.-156+1017_-156+1022del	N/A	Intron Variant
ZNF559 transcript variant 8	NM_001202412.2:c.-120+101… NM_001202412.2:c.-120+1017_-120+1022del	N/A	Intron Variant
ZNF559 transcript variant 2	NM_032497.3:c.-120+1017_-… NM_032497.3:c.-120+1017_-120+1022del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₁₆=	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₈
GRCh38.p14 chr 19	NC_000019.10:g.9325787_9325802=	NC_000019.10:g.9325797_9325802del	NC_000019.10:g.9325798_9325802del	NC_000019.10:g.9325799_9325802del	NC_000019.10:g.9325800_9325802del	NC_000019.10:g.9325801_9325802del	NC_000019.10:g.9325802del	NC_000019.10:g.9325802dup	NC_000019.10:g.9325800_9325802dup	NC_000019.10:g.9325799_9325802dup	NC_000019.10:g.9325798_9325802dup	NC_000019.10:g.9325795_9325802dup
GRCh37.p13 chr 19	NC_000019.9:g.9436463_9436478=	NC_000019.9:g.9436473_9436478del	NC_000019.9:g.9436474_9436478del	NC_000019.9:g.9436475_9436478del	NC_000019.9:g.9436476_9436478del	NC_000019.9:g.9436477_9436478del	NC_000019.9:g.9436478del	NC_000019.9:g.9436478dup	NC_000019.9:g.9436476_9436478dup	NC_000019.9:g.9436475_9436478dup	NC_000019.9:g.9436474_9436478dup	NC_000019.9:g.9436471_9436478dup
ZNF559-ZNF177 transcript variant 2	NM_001172650.2:c.-480+1007=	NM_001172650.2:c.-480+1017_-480+1022del	NM_001172650.2:c.-480+1018_-480+1022del	NM_001172650.2:c.-480+1019_-480+1022del	NM_001172650.2:c.-480+1020_-480+1022del	NM_001172650.2:c.-480+1021_-480+1022del	NM_001172650.2:c.-480+1022del	NM_001172650.2:c.-480+1022dup	NM_001172650.2:c.-480+1020_-480+1022dup	NM_001172650.2:c.-480+1019_-480+1022dup	NM_001172650.2:c.-480+1018_-480+1022dup	NM_001172650.2:c.-480+1015_-480+1022dup
ZNF559-ZNF177 transcript variant 2	NM_001172650.3:c.-480+1007=	NM_001172650.3:c.-480+1017_-480+1022del	NM_001172650.3:c.-480+1018_-480+1022del	NM_001172650.3:c.-480+1019_-480+1022del	NM_001172650.3:c.-480+1020_-480+1022del	NM_001172650.3:c.-480+1021_-480+1022del	NM_001172650.3:c.-480+1022del	NM_001172650.3:c.-480+1022dup	NM_001172650.3:c.-480+1020_-480+1022dup	NM_001172650.3:c.-480+1019_-480+1022dup	NM_001172650.3:c.-480+1018_-480+1022dup	NM_001172650.3:c.-480+1015_-480+1022dup
ZNF559 transcript variant 1	NM_001202406.1:c.136+1007=	NM_001202406.1:c.136+1017_136+1022del	NM_001202406.1:c.136+1018_136+1022del	NM_001202406.1:c.136+1019_136+1022del	NM_001202406.1:c.136+1020_136+1022del	NM_001202406.1:c.136+1021_136+1022del	NM_001202406.1:c.136+1022del	NM_001202406.1:c.136+1022dup	NM_001202406.1:c.136+1020_136+1022dup	NM_001202406.1:c.136+1019_136+1022dup	NM_001202406.1:c.136+1018_136+1022dup	NM_001202406.1:c.136+1015_136+1022dup
ZNF559 transcript variant 3	NM_001202407.1:c.-193+1007=	NM_001202407.1:c.-193+1017_-193+1022del	NM_001202407.1:c.-193+1018_-193+1022del	NM_001202407.1:c.-193+1019_-193+1022del	NM_001202407.1:c.-193+1020_-193+1022del	NM_001202407.1:c.-193+1021_-193+1022del	NM_001202407.1:c.-193+1022del	NM_001202407.1:c.-193+1022dup	NM_001202407.1:c.-193+1020_-193+1022dup	NM_001202407.1:c.-193+1019_-193+1022dup	NM_001202407.1:c.-193+1018_-193+1022dup	NM_001202407.1:c.-193+1015_-193+1022dup
ZNF559 transcript variant 3	NM_001202407.3:c.-193+1007=	NM_001202407.3:c.-193+1017_-193+1022del	NM_001202407.3:c.-193+1018_-193+1022del	NM_001202407.3:c.-193+1019_-193+1022del	NM_001202407.3:c.-193+1020_-193+1022del	NM_001202407.3:c.-193+1021_-193+1022del	NM_001202407.3:c.-193+1022del	NM_001202407.3:c.-193+1022dup	NM_001202407.3:c.-193+1020_-193+1022dup	NM_001202407.3:c.-193+1019_-193+1022dup	NM_001202407.3:c.-193+1018_-193+1022dup	NM_001202407.3:c.-193+1015_-193+1022dup
ZNF559 transcript variant 4	NM_001202408.1:c.136+1007=	NM_001202408.1:c.136+1017_136+1022del	NM_001202408.1:c.136+1018_136+1022del	NM_001202408.1:c.136+1019_136+1022del	NM_001202408.1:c.136+1020_136+1022del	NM_001202408.1:c.136+1021_136+1022del	NM_001202408.1:c.136+1022del	NM_001202408.1:c.136+1022dup	NM_001202408.1:c.136+1020_136+1022dup	NM_001202408.1:c.136+1019_136+1022dup	NM_001202408.1:c.136+1018_136+1022dup	NM_001202408.1:c.136+1015_136+1022dup
ZNF559 transcript variant 5	NM_001202409.1:c.-195+1007=	NM_001202409.1:c.-195+1017_-195+1022del	NM_001202409.1:c.-195+1018_-195+1022del	NM_001202409.1:c.-195+1019_-195+1022del	NM_001202409.1:c.-195+1020_-195+1022del	NM_001202409.1:c.-195+1021_-195+1022del	NM_001202409.1:c.-195+1022del	NM_001202409.1:c.-195+1022dup	NM_001202409.1:c.-195+1020_-195+1022dup	NM_001202409.1:c.-195+1019_-195+1022dup	NM_001202409.1:c.-195+1018_-195+1022dup	NM_001202409.1:c.-195+1015_-195+1022dup
ZNF559 transcript variant 5	NM_001202409.2:c.-195+1007=	NM_001202409.2:c.-195+1017_-195+1022del	NM_001202409.2:c.-195+1018_-195+1022del	NM_001202409.2:c.-195+1019_-195+1022del	NM_001202409.2:c.-195+1020_-195+1022del	NM_001202409.2:c.-195+1021_-195+1022del	NM_001202409.2:c.-195+1022del	NM_001202409.2:c.-195+1022dup	NM_001202409.2:c.-195+1020_-195+1022dup	NM_001202409.2:c.-195+1019_-195+1022dup	NM_001202409.2:c.-195+1018_-195+1022dup	NM_001202409.2:c.-195+1015_-195+1022dup
ZNF559 transcript variant 6	NM_001202410.1:c.-127+1007=	NM_001202410.1:c.-127+1017_-127+1022del	NM_001202410.1:c.-127+1018_-127+1022del	NM_001202410.1:c.-127+1019_-127+1022del	NM_001202410.1:c.-127+1020_-127+1022del	NM_001202410.1:c.-127+1021_-127+1022del	NM_001202410.1:c.-127+1022del	NM_001202410.1:c.-127+1022dup	NM_001202410.1:c.-127+1020_-127+1022dup	NM_001202410.1:c.-127+1019_-127+1022dup	NM_001202410.1:c.-127+1018_-127+1022dup	NM_001202410.1:c.-127+1015_-127+1022dup
ZNF559 transcript variant 6	NM_001202410.2:c.-127+1007=	NM_001202410.2:c.-127+1017_-127+1022del	NM_001202410.2:c.-127+1018_-127+1022del	NM_001202410.2:c.-127+1019_-127+1022del	NM_001202410.2:c.-127+1020_-127+1022del	NM_001202410.2:c.-127+1021_-127+1022del	NM_001202410.2:c.-127+1022del	NM_001202410.2:c.-127+1022dup	NM_001202410.2:c.-127+1020_-127+1022dup	NM_001202410.2:c.-127+1019_-127+1022dup	NM_001202410.2:c.-127+1018_-127+1022dup	NM_001202410.2:c.-127+1015_-127+1022dup
ZNF559 transcript variant 7	NM_001202411.1:c.-156+1007=	NM_001202411.1:c.-156+1017_-156+1022del	NM_001202411.1:c.-156+1018_-156+1022del	NM_001202411.1:c.-156+1019_-156+1022del	NM_001202411.1:c.-156+1020_-156+1022del	NM_001202411.1:c.-156+1021_-156+1022del	NM_001202411.1:c.-156+1022del	NM_001202411.1:c.-156+1022dup	NM_001202411.1:c.-156+1020_-156+1022dup	NM_001202411.1:c.-156+1019_-156+1022dup	NM_001202411.1:c.-156+1018_-156+1022dup	NM_001202411.1:c.-156+1015_-156+1022dup
ZNF559 transcript variant 7	NM_001202411.2:c.-156+1007=	NM_001202411.2:c.-156+1017_-156+1022del	NM_001202411.2:c.-156+1018_-156+1022del	NM_001202411.2:c.-156+1019_-156+1022del	NM_001202411.2:c.-156+1020_-156+1022del	NM_001202411.2:c.-156+1021_-156+1022del	NM_001202411.2:c.-156+1022del	NM_001202411.2:c.-156+1022dup	NM_001202411.2:c.-156+1020_-156+1022dup	NM_001202411.2:c.-156+1019_-156+1022dup	NM_001202411.2:c.-156+1018_-156+1022dup	NM_001202411.2:c.-156+1015_-156+1022dup
ZNF559 transcript variant 8	NM_001202412.1:c.-120+1007=	NM_001202412.1:c.-120+1017_-120+1022del	NM_001202412.1:c.-120+1018_-120+1022del	NM_001202412.1:c.-120+1019_-120+1022del	NM_001202412.1:c.-120+1020_-120+1022del	NM_001202412.1:c.-120+1021_-120+1022del	NM_001202412.1:c.-120+1022del	NM_001202412.1:c.-120+1022dup	NM_001202412.1:c.-120+1020_-120+1022dup	NM_001202412.1:c.-120+1019_-120+1022dup	NM_001202412.1:c.-120+1018_-120+1022dup	NM_001202412.1:c.-120+1015_-120+1022dup
ZNF559 transcript variant 8	NM_001202412.2:c.-120+1007=	NM_001202412.2:c.-120+1017_-120+1022del	NM_001202412.2:c.-120+1018_-120+1022del	NM_001202412.2:c.-120+1019_-120+1022del	NM_001202412.2:c.-120+1020_-120+1022del	NM_001202412.2:c.-120+1021_-120+1022del	NM_001202412.2:c.-120+1022del	NM_001202412.2:c.-120+1022dup	NM_001202412.2:c.-120+1020_-120+1022dup	NM_001202412.2:c.-120+1019_-120+1022dup	NM_001202412.2:c.-120+1018_-120+1022dup	NM_001202412.2:c.-120+1015_-120+1022dup
ZNF559-ZNF177 transcript variant 4	NM_001202425.1:c.-392+1007=	NM_001202425.1:c.-392+1017_-392+1022del	NM_001202425.1:c.-392+1018_-392+1022del	NM_001202425.1:c.-392+1019_-392+1022del	NM_001202425.1:c.-392+1020_-392+1022del	NM_001202425.1:c.-392+1021_-392+1022del	NM_001202425.1:c.-392+1022del	NM_001202425.1:c.-392+1022dup	NM_001202425.1:c.-392+1020_-392+1022dup	NM_001202425.1:c.-392+1019_-392+1022dup	NM_001202425.1:c.-392+1018_-392+1022dup	NM_001202425.1:c.-392+1015_-392+1022dup
ZNF559-ZNF177 transcript variant 5	NM_001384659.1:c.-770+1007=	NM_001384659.1:c.-770+1017_-770+1022del	NM_001384659.1:c.-770+1018_-770+1022del	NM_001384659.1:c.-770+1019_-770+1022del	NM_001384659.1:c.-770+1020_-770+1022del	NM_001384659.1:c.-770+1021_-770+1022del	NM_001384659.1:c.-770+1022del	NM_001384659.1:c.-770+1022dup	NM_001384659.1:c.-770+1020_-770+1022dup	NM_001384659.1:c.-770+1019_-770+1022dup	NM_001384659.1:c.-770+1018_-770+1022dup	NM_001384659.1:c.-770+1015_-770+1022dup
ZNF559 transcript variant 2	NM_032497.2:c.-120+1007=	NM_032497.2:c.-120+1017_-120+1022del	NM_032497.2:c.-120+1018_-120+1022del	NM_032497.2:c.-120+1019_-120+1022del	NM_032497.2:c.-120+1020_-120+1022del	NM_032497.2:c.-120+1021_-120+1022del	NM_032497.2:c.-120+1022del	NM_032497.2:c.-120+1022dup	NM_032497.2:c.-120+1020_-120+1022dup	NM_032497.2:c.-120+1019_-120+1022dup	NM_032497.2:c.-120+1018_-120+1022dup	NM_032497.2:c.-120+1015_-120+1022dup
ZNF559 transcript variant 2	NM_032497.3:c.-120+1007=	NM_032497.3:c.-120+1017_-120+1022del	NM_032497.3:c.-120+1018_-120+1022del	NM_032497.3:c.-120+1019_-120+1022del	NM_032497.3:c.-120+1020_-120+1022del	NM_032497.3:c.-120+1021_-120+1022del	NM_032497.3:c.-120+1022del	NM_032497.3:c.-120+1022dup	NM_032497.3:c.-120+1020_-120+1022dup	NM_032497.3:c.-120+1019_-120+1022dup	NM_032497.3:c.-120+1018_-120+1022dup	NM_032497.3:c.-120+1015_-120+1022dup
ZNF559 transcript variant X1	XM_005260102.1:c.-195+1007=	XM_005260102.1:c.-195+1017_-195+1022del	XM_005260102.1:c.-195+1018_-195+1022del	XM_005260102.1:c.-195+1019_-195+1022del	XM_005260102.1:c.-195+1020_-195+1022del	XM_005260102.1:c.-195+1021_-195+1022del	XM_005260102.1:c.-195+1022del	XM_005260102.1:c.-195+1022dup	XM_005260102.1:c.-195+1020_-195+1022dup	XM_005260102.1:c.-195+1019_-195+1022dup	XM_005260102.1:c.-195+1018_-195+1022dup	XM_005260102.1:c.-195+1015_-195+1022dup
ZNF559 transcript variant X2	XM_005260103.1:c.-195+1007=	XM_005260103.1:c.-195+1017_-195+1022del	XM_005260103.1:c.-195+1018_-195+1022del	XM_005260103.1:c.-195+1019_-195+1022del	XM_005260103.1:c.-195+1020_-195+1022del	XM_005260103.1:c.-195+1021_-195+1022del	XM_005260103.1:c.-195+1022del	XM_005260103.1:c.-195+1022dup	XM_005260103.1:c.-195+1020_-195+1022dup	XM_005260103.1:c.-195+1019_-195+1022dup	XM_005260103.1:c.-195+1018_-195+1022dup	XM_005260103.1:c.-195+1015_-195+1022dup
ZNF559 transcript variant X3	XM_005260104.1:c.-120+1007=	XM_005260104.1:c.-120+1017_-120+1022del	XM_005260104.1:c.-120+1018_-120+1022del	XM_005260104.1:c.-120+1019_-120+1022del	XM_005260104.1:c.-120+1020_-120+1022del	XM_005260104.1:c.-120+1021_-120+1022del	XM_005260104.1:c.-120+1022del	XM_005260104.1:c.-120+1022dup	XM_005260104.1:c.-120+1020_-120+1022dup	XM_005260104.1:c.-120+1019_-120+1022dup	XM_005260104.1:c.-120+1018_-120+1022dup	XM_005260104.1:c.-120+1015_-120+1022dup
ZNF559 transcript variant X4	XM_005260105.1:c.-57+1007=	XM_005260105.1:c.-57+1017_-57+1022del	XM_005260105.1:c.-57+1018_-57+1022del	XM_005260105.1:c.-57+1019_-57+1022del	XM_005260105.1:c.-57+1020_-57+1022del	XM_005260105.1:c.-57+1021_-57+1022del	XM_005260105.1:c.-57+1022del	XM_005260105.1:c.-57+1022dup	XM_005260105.1:c.-57+1020_-57+1022dup	XM_005260105.1:c.-57+1019_-57+1022dup	XM_005260105.1:c.-57+1018_-57+1022dup	XM_005260105.1:c.-57+1015_-57+1022dup
ZNF559 transcript variant X5	XM_005260106.1:c.-94+1007=	XM_005260106.1:c.-94+1017_-94+1022del	XM_005260106.1:c.-94+1018_-94+1022del	XM_005260106.1:c.-94+1019_-94+1022del	XM_005260106.1:c.-94+1020_-94+1022del	XM_005260106.1:c.-94+1021_-94+1022del	XM_005260106.1:c.-94+1022del	XM_005260106.1:c.-94+1022dup	XM_005260106.1:c.-94+1020_-94+1022dup	XM_005260106.1:c.-94+1019_-94+1022dup	XM_005260106.1:c.-94+1018_-94+1022dup	XM_005260106.1:c.-94+1015_-94+1022dup
ZNF559 transcript variant X6	XM_005260107.1:c.-392+1007=	XM_005260107.1:c.-392+1017_-392+1022del	XM_005260107.1:c.-392+1018_-392+1022del	XM_005260107.1:c.-392+1019_-392+1022del	XM_005260107.1:c.-392+1020_-392+1022del	XM_005260107.1:c.-392+1021_-392+1022del	XM_005260107.1:c.-392+1022del	XM_005260107.1:c.-392+1022dup	XM_005260107.1:c.-392+1020_-392+1022dup	XM_005260107.1:c.-392+1019_-392+1022dup	XM_005260107.1:c.-392+1018_-392+1022dup	XM_005260107.1:c.-392+1015_-392+1022dup
ZNF559 transcript variant X7	XM_005260108.1:c.-81+1007=	XM_005260108.1:c.-81+1017_-81+1022del	XM_005260108.1:c.-81+1018_-81+1022del	XM_005260108.1:c.-81+1019_-81+1022del	XM_005260108.1:c.-81+1020_-81+1022del	XM_005260108.1:c.-81+1021_-81+1022del	XM_005260108.1:c.-81+1022del	XM_005260108.1:c.-81+1022dup	XM_005260108.1:c.-81+1020_-81+1022dup	XM_005260108.1:c.-81+1019_-81+1022dup	XM_005260108.1:c.-81+1018_-81+1022dup	XM_005260108.1:c.-81+1015_-81+1022dup
ZNF559 transcript variant X8	XM_005260109.1:c.-180+1007=	XM_005260109.1:c.-180+1017_-180+1022del	XM_005260109.1:c.-180+1018_-180+1022del	XM_005260109.1:c.-180+1019_-180+1022del	XM_005260109.1:c.-180+1020_-180+1022del	XM_005260109.1:c.-180+1021_-180+1022del	XM_005260109.1:c.-180+1022del	XM_005260109.1:c.-180+1022dup	XM_005260109.1:c.-180+1020_-180+1022dup	XM_005260109.1:c.-180+1019_-180+1022dup	XM_005260109.1:c.-180+1018_-180+1022dup	XM_005260109.1:c.-180+1015_-180+1022dup
ZNF559 transcript variant X9	XM_005260110.1:c.-891+1007=	XM_005260110.1:c.-891+1017_-891+1022del	XM_005260110.1:c.-891+1018_-891+1022del	XM_005260110.1:c.-891+1019_-891+1022del	XM_005260110.1:c.-891+1020_-891+1022del	XM_005260110.1:c.-891+1021_-891+1022del	XM_005260110.1:c.-891+1022del	XM_005260110.1:c.-891+1022dup	XM_005260110.1:c.-891+1020_-891+1022dup	XM_005260110.1:c.-891+1019_-891+1022dup	XM_005260110.1:c.-891+1018_-891+1022dup	XM_005260110.1:c.-891+1015_-891+1022dup
ZNF559 transcript variant X10	XM_005260111.1:c.-891+1007=	XM_005260111.1:c.-891+1017_-891+1022del	XM_005260111.1:c.-891+1018_-891+1022del	XM_005260111.1:c.-891+1019_-891+1022del	XM_005260111.1:c.-891+1020_-891+1022del	XM_005260111.1:c.-891+1021_-891+1022del	XM_005260111.1:c.-891+1022del	XM_005260111.1:c.-891+1022dup	XM_005260111.1:c.-891+1020_-891+1022dup	XM_005260111.1:c.-891+1019_-891+1022dup	XM_005260111.1:c.-891+1018_-891+1022dup	XM_005260111.1:c.-891+1015_-891+1022dup
ZNF559 transcript variant X11	XM_005260112.1:c.-1050+1007=	XM_005260112.1:c.-1050+1017_-1050+1022del	XM_005260112.1:c.-1050+1018_-1050+1022del	XM_005260112.1:c.-1050+1019_-1050+1022del	XM_005260112.1:c.-1050+1020_-1050+1022del	XM_005260112.1:c.-1050+1021_-1050+1022del	XM_005260112.1:c.-1050+1022del	XM_005260112.1:c.-1050+1022dup	XM_005260112.1:c.-1050+1020_-1050+1022dup	XM_005260112.1:c.-1050+1019_-1050+1022dup	XM_005260112.1:c.-1050+1018_-1050+1022dup	XM_005260112.1:c.-1050+1015_-1050+1022dup
ZNF559 transcript variant X12	XM_005260113.1:c.-898+1007=	XM_005260113.1:c.-898+1017_-898+1022del	XM_005260113.1:c.-898+1018_-898+1022del	XM_005260113.1:c.-898+1019_-898+1022del	XM_005260113.1:c.-898+1020_-898+1022del	XM_005260113.1:c.-898+1021_-898+1022del	XM_005260113.1:c.-898+1022del	XM_005260113.1:c.-898+1022dup	XM_005260113.1:c.-898+1020_-898+1022dup	XM_005260113.1:c.-898+1019_-898+1022dup	XM_005260113.1:c.-898+1018_-898+1022dup	XM_005260113.1:c.-898+1015_-898+1022dup
ZNF559 transcript variant X13	XM_005260114.1:c.-927+1007=	XM_005260114.1:c.-927+1017_-927+1022del	XM_005260114.1:c.-927+1018_-927+1022del	XM_005260114.1:c.-927+1019_-927+1022del	XM_005260114.1:c.-927+1020_-927+1022del	XM_005260114.1:c.-927+1021_-927+1022del	XM_005260114.1:c.-927+1022del	XM_005260114.1:c.-927+1022dup	XM_005260114.1:c.-927+1020_-927+1022dup	XM_005260114.1:c.-927+1019_-927+1022dup	XM_005260114.1:c.-927+1018_-927+1022dup	XM_005260114.1:c.-927+1015_-927+1022dup
ZNF559 transcript variant X14	XM_005260115.1:c.-711+1007=	XM_005260115.1:c.-711+1017_-711+1022del	XM_005260115.1:c.-711+1018_-711+1022del	XM_005260115.1:c.-711+1019_-711+1022del	XM_005260115.1:c.-711+1020_-711+1022del	XM_005260115.1:c.-711+1021_-711+1022del	XM_005260115.1:c.-711+1022del	XM_005260115.1:c.-711+1022dup	XM_005260115.1:c.-711+1020_-711+1022dup	XM_005260115.1:c.-711+1019_-711+1022dup	XM_005260115.1:c.-711+1018_-711+1022dup	XM_005260115.1:c.-711+1015_-711+1022dup
ZNF559 transcript variant X15	XM_005260116.1:c.-195+1007=	XM_005260116.1:c.-195+1017_-195+1022del	XM_005260116.1:c.-195+1018_-195+1022del	XM_005260116.1:c.-195+1019_-195+1022del	XM_005260116.1:c.-195+1020_-195+1022del	XM_005260116.1:c.-195+1021_-195+1022del	XM_005260116.1:c.-195+1022del	XM_005260116.1:c.-195+1022dup	XM_005260116.1:c.-195+1020_-195+1022dup	XM_005260116.1:c.-195+1019_-195+1022dup	XM_005260116.1:c.-195+1018_-195+1022dup	XM_005260116.1:c.-195+1015_-195+1022dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

67 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40980346	Mar 15, 2016 (147)
2	HGSV	ss77841427	Sep 08, 2015 (146)
3	HGSV	ss77842024	Sep 08, 2015 (146)
4	HGSV	ss77871829	Sep 08, 2015 (146)
5	HGSV	ss81643207	Sep 08, 2015 (146)
6	HGSV	ss82223882	Sep 08, 2015 (146)
7	HUMANGENOME_JCVI	ss95721477	Dec 05, 2013 (138)
8	BUSHMAN	ss193497293	Mar 15, 2016 (147)
9	BL	ss256192359	May 09, 2011 (137)
10	GMI	ss289375609	May 04, 2012 (137)
11	GMI	ss289375610	May 04, 2012 (137)
12	PJP	ss294953518	May 09, 2011 (135)
13	BILGI_BIOE	ss666724115	Apr 25, 2013 (138)
14	1000GENOMES	ss1377935541	Aug 21, 2014 (142)
15	EVA_UK10K_TWINSUK	ss1709117370	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1709117426	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1710779457	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1710779458	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1710779459	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1710779460	Apr 01, 2015 (144)
21	SWEGEN	ss3017083066	Nov 08, 2017 (151)
22	MCHAISSO	ss3064754168	Nov 08, 2017 (151)
23	MCHAISSO	ss3065700306	Nov 08, 2017 (151)
24	BEROUKHIMLAB	ss3644432927	Oct 12, 2018 (152)
25	BIOINF_KMB_FNS_UNIBA	ss3645507860	Oct 12, 2018 (152)
26	BIOINF_KMB_FNS_UNIBA	ss3645507861	Oct 12, 2018 (152)
27	EVA_DECODE	ss3702326625	Jul 13, 2019 (153)
28	EVA_DECODE	ss3702326626	Jul 13, 2019 (153)
29	EVA_DECODE	ss3702326627	Jul 13, 2019 (153)
30	EVA_DECODE	ss3702326628	Jul 13, 2019 (153)
31	EVA_DECODE	ss3702326629	Jul 13, 2019 (153)
32	PACBIO	ss3788465825	Jul 13, 2019 (153)
33	PACBIO	ss3788465826	Jul 13, 2019 (153)
34	PACBIO	ss3793386458	Jul 13, 2019 (153)
35	PACBIO	ss3793386459	Jul 13, 2019 (153)
36	PACBIO	ss3798273105	Jul 13, 2019 (153)
37	PACBIO	ss3798273106	Jul 13, 2019 (153)
38	KHV_HUMAN_GENOMES	ss3821056149	Jul 13, 2019 (153)
39	EVA	ss3835347488	Apr 27, 2020 (154)
40	KOGIC	ss3980814783	Apr 27, 2020 (154)
41	KOGIC	ss3980814784	Apr 27, 2020 (154)
42	KOGIC	ss3980814785	Apr 27, 2020 (154)
43	GNOMAD	ss4327495783	Apr 27, 2021 (155)
44	GNOMAD	ss4327495784	Apr 27, 2021 (155)
45	GNOMAD	ss4327495785	Apr 27, 2021 (155)
46	GNOMAD	ss4327495786	Apr 27, 2021 (155)
47	GNOMAD	ss4327495787	Apr 27, 2021 (155)
48	GNOMAD	ss4327495788	Apr 27, 2021 (155)
49	GNOMAD	ss4327495789	Apr 27, 2021 (155)
50	GNOMAD	ss4327495790	Apr 27, 2021 (155)
51	GNOMAD	ss4327495791	Apr 27, 2021 (155)
52	TOMMO_GENOMICS	ss5226697726	Apr 27, 2021 (155)
53	TOMMO_GENOMICS	ss5226697727	Apr 27, 2021 (155)
54	TOMMO_GENOMICS	ss5226697728	Apr 27, 2021 (155)
55	TOMMO_GENOMICS	ss5226697729	Apr 27, 2021 (155)
56	1000G_HIGH_COVERAGE	ss5306461072	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5499094245	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5499094246	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5784962734	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5784962735	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5784962736	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5784962737	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5784962738	Oct 16, 2022 (156)
64	EVA	ss5840242514	Oct 16, 2022 (156)
65	EVA	ss5840242515	Oct 16, 2022 (156)
66	EVA	ss5840242516	Oct 16, 2022 (156)
67	EVA	ss5927262228	Oct 16, 2022 (156)
68	1000Genomes	NC_000019.9 - 9436463	Oct 12, 2018 (152)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 41941029 (NC_000019.9:9436463:A: 1950/3854) Row 41941031 (NC_000019.9:9436462:AAA: 223/3854)	-	Oct 12, 2018 (152)
70	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 41941029 (NC_000019.9:9436463:A: 1950/3854) Row 41941031 (NC_000019.9:9436462:AAA: 223/3854)	-	Oct 12, 2018 (152)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533803623 (NC_000019.10:9325786::A 2/127884) Row 533803624 (NC_000019.10:9325786::AAA 1/127892) Row 533803625 (NC_000019.10:9325786::AAAA 8/127894)...	-	Apr 27, 2021 (155)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 37192784 (NC_000019.10:9325787:AA: 1073/1832) Row 37192785 (NC_000019.10:9325788:A: 632/1832) Row 37192786 (NC_000019.10:9325786:AAA: 39/1832)	-	Apr 27, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 37192784 (NC_000019.10:9325787:AA: 1073/1832) Row 37192785 (NC_000019.10:9325788:A: 632/1832) Row 37192786 (NC_000019.10:9325786:AAA: 39/1832)	-	Apr 27, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 37192784 (NC_000019.10:9325787:AA: 1073/1832) Row 37192785 (NC_000019.10:9325788:A: 632/1832) Row 37192786 (NC_000019.10:9325786:AAA: 39/1832)	-	Apr 27, 2020 (154)
84	8.3KJPN Submission ignored due to conflicting rows: Row 84667033 (NC_000019.9:9436462:AA: 11088/16754) Row 84667034 (NC_000019.9:9436462:A: 5086/16754) Row 84667035 (NC_000019.9:9436462:AAA: 24/16754)...	-	Apr 27, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 84667033 (NC_000019.9:9436462:AA: 11088/16754) Row 84667034 (NC_000019.9:9436462:A: 5086/16754) Row 84667035 (NC_000019.9:9436462:AAA: 24/16754)...	-	Apr 27, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 84667033 (NC_000019.9:9436462:AA: 11088/16754) Row 84667034 (NC_000019.9:9436462:A: 5086/16754) Row 84667035 (NC_000019.9:9436462:AAA: 24/16754)...	-	Apr 27, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 84667033 (NC_000019.9:9436462:AA: 11088/16754) Row 84667034 (NC_000019.9:9436462:A: 5086/16754) Row 84667035 (NC_000019.9:9436462:AAA: 24/16754)...	-	Apr 27, 2021 (155)
88	14KJPN Submission ignored due to conflicting rows: Row 118799838 (NC_000019.10:9325786:AA: 18785/28258) Row 118799839 (NC_000019.10:9325786:A: 8550/28258) Row 118799840 (NC_000019.10:9325786:AAA: 32/28258)...	-	Oct 16, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 118799838 (NC_000019.10:9325786:AA: 18785/28258) Row 118799839 (NC_000019.10:9325786:A: 8550/28258) Row 118799840 (NC_000019.10:9325786:AAA: 32/28258)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 118799838 (NC_000019.10:9325786:AA: 18785/28258) Row 118799839 (NC_000019.10:9325786:A: 8550/28258) Row 118799840 (NC_000019.10:9325786:AAA: 32/28258)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 118799838 (NC_000019.10:9325786:AA: 18785/28258) Row 118799839 (NC_000019.10:9325786:A: 8550/28258) Row 118799840 (NC_000019.10:9325786:AAA: 32/28258)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 118799838 (NC_000019.10:9325786:AA: 18785/28258) Row 118799839 (NC_000019.10:9325786:A: 8550/28258) Row 118799840 (NC_000019.10:9325786:AAA: 32/28258)...	-	Oct 16, 2022 (156)
93	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41941029 (NC_000019.9:9436463:A: 1883/3708) Row 41941031 (NC_000019.9:9436462:AAA: 197/3708)	-	Oct 12, 2018 (152)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41941029 (NC_000019.9:9436463:AA: 1883/3708) Row 41941030 (NC_000019.9:9436464:A: 1628/3708) Row 41941031 (NC_000019.9:9436462:AAA: 197/3708)	-	Apr 27, 2020 (154)
95	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41941029 (NC_000019.9:9436463:A: 1883/3708) Row 41941031 (NC_000019.9:9436462:AAA: 197/3708)	-	Oct 12, 2018 (152)
96	ALFA	NC_000019.10 - 9325787	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs58096074	Dec 02, 2009 (131)
rs148771184	Sep 17, 2011 (135)
rs200919523	May 11, 2012 (137)
rs35901278	May 23, 2006 (127)
rs112409590	May 11, 2012 (137)
rs139080800	May 04, 2012 (137)
rs373690253	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5226697729	NC_000019.9:9436462:AAAAAA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4327495791, ss5784962738	NC_000019.10:9325786:AAAAAA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4327495790	NC_000019.10:9325786:AAAAA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3017083066	NC_000019.9:9436462:AAAA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3702326629, ss4327495789, ss5784962737	NC_000019.10:9325786:AAAA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss1709117370, ss1709117426, ss5226697728, ss5840242516	NC_000019.9:9436462:AAA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3065700306, ss3980814785, ss4327495788, ss5306461072, ss5784962736	NC_000019.10:9325786:AAA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3702326628	NC_000019.10:9325787:AAA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss289375610	NC_000019.8:9297462:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss77841427, ss77842024, ss77871829, ss81643207, ss82223882, ss294953518	NC_000019.8:9297476:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
75692019, ss1377935541, ss3788465826, ss3793386458, ss3798273105, ss3835347488, ss5226697726, ss5840242514	NC_000019.9:9436462:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1710779457, ss1710779458	NC_000019.9:9436463:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3064754168, ss3645507860, ss3821056149, ss4327495787, ss5499094245, ss5784962734, ss5927262228	NC_000019.10:9325786:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3980814783	NC_000019.10:9325787:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3702326627	NC_000019.10:9325788:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss40980346, ss193497293	NT_011295.11:699264:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss95721477	NT_011295.11:699278:AA:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss256192359, ss289375609	NC_000019.8:9297462:A:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss666724115, ss3644432927, ss3788465825, ss3793386459, ss3798273106, ss5226697727, ss5840242515	NC_000019.9:9436462:A:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
	NC_000019.9:9436463:A:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss1710779459, ss1710779460	NC_000019.9:9436464:A:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3645507861, ss5499094246, ss5784962735	NC_000019.10:9325786:A:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3980814784	NC_000019.10:9325788:A:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3702326626	NC_000019.10:9325789:A:	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss40980346	NT_011295.11:699264:AA:A	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4327495783	NC_000019.10:9325786::A	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4327495784	NC_000019.10:9325786::AAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4327495785	NC_000019.10:9325786::AAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4327495786	NC_000019.10:9325786::AAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
5395804831	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3702326625	NC_000019.10:9325790::AAAAAAAA	NC_000019.10:9325786:AAAAAAAAAAAAA… NC_000019.10:9325786:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs35775585

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35775585