Name: rs143742416
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.

rs143742416

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:170286803-170286826 (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(AC)₆ / del(AC)₅ / del(AC)₄ / d…
del(AC)₆ / del(AC)₅ / del(AC)₄ / del(AC)₃ / delACAC / delAC / dupAC / dupACAC / dup(AC)₃ / dup(AC)₄ / dup(AC)₅ / dup(AC)₉
Variation Type: Indel Insertion and Deletion
Frequency: delAC=0.03514 (533/15166, ALFA)
delAC=0.3073 (1539/5008, 1000G)
delAC=0.30 (12/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DLL1 : 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	15166	ACACACACACACACACACACACAC=0.95793	ACACACACACAC=0.00000, ACACACACACACAC=0.00000, ACACACACACACACAC=0.00000, ACACACACACACACACAC=0.00007, ACACACACACACACACACAC=0.00284, ACACACACACACACACACACAC=0.03514, ACACACACACACACACACACACACAC=0.00330, ACACACACACACACACACACACACACACAC=0.00073, ACACACACACACACACACACACACACAC=0.00000, ACACACACACACACACACACACACACACACAC=0.00000, ACACACACACACACACACACACACACACACACAC=0.00000, ACACACACACACACACACACACACACACACACACACACACAC=0.00000	0.934109	0.004544	0.061347	32
European	Sub	12718	ACACACACACACACACACACACAC=0.94991	ACACACACACAC=0.00000, ACACACACACACAC=0.00000, ACACACACACACACAC=0.00000, ACACACACACACACACAC=0.00008, ACACACACACACACACACAC=0.00338, ACACACACACACACACACACAC=0.04191, ACACACACACACACACACACACACAC=0.00393, ACACACACACACACACACACACACACACAC=0.00079, ACACACACACACACACACACACACACAC=0.00000, ACACACACACACACACACACACACACACACAC=0.00000, ACACACACACACACACACACACACACACACACAC=0.00000, ACACACACACACACACACACACACACACACACACACACACAC=0.00000	0.921233	0.005432	0.073334	27
African	Sub	1550	ACACACACACACACACACACACAC=1.0000	ACACACACACAC=0.0000, ACACACACACACAC=0.0000, ACACACACACACACAC=0.0000, ACACACACACACACACAC=0.0000, ACACACACACACACACACAC=0.0000, ACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACACACACACACACACAC=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	60	ACACACACACACACACACACACAC=1.00	ACACACACACAC=0.00, ACACACACACACAC=0.00, ACACACACACACACAC=0.00, ACACACACACACACACAC=0.00, ACACACACACACACACACAC=0.00, ACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
African American	Sub	1490	ACACACACACACACACACACACAC=1.0000	ACACACACACAC=0.0000, ACACACACACACAC=0.0000, ACACACACACACACAC=0.0000, ACACACACACACACACAC=0.0000, ACACACACACACACACACAC=0.0000, ACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACACACACAC=0.0000, ACACACACACACACACACACACACACACACACACACACACAC=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	24	ACACACACACACACACACACACAC=1.00	ACACACACACAC=0.00, ACACACACACACAC=0.00, ACACACACACACACAC=0.00, ACACACACACACACACAC=0.00, ACACACACACACACACACAC=0.00, ACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	ACACACACACACACACACACACAC=1.00	ACACACACACAC=0.00, ACACACACACACAC=0.00, ACACACACACACACAC=0.00, ACACACACACACACACAC=0.00, ACACACACACACACACACAC=0.00, ACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	ACACACACACACACACACACACAC=1.0	ACACACACACAC=0.0, ACACACACACACAC=0.0, ACACACACACACACAC=0.0, ACACACACACACACACAC=0.0, ACACACACACACACACACAC=0.0, ACACACACACACACACACACAC=0.0, ACACACACACACACACACACACACAC=0.0, ACACACACACACACACACACACACACACAC=0.0, ACACACACACACACACACACACACACAC=0.0, ACACACACACACACACACACACACACACACAC=0.0, ACACACACACACACACACACACACACACACACAC=0.0, ACACACACACACACACACACACACACACACACACACACACAC=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	110	ACACACACACACACACACACACAC=1.000	ACACACACACAC=0.000, ACACACACACACAC=0.000, ACACACACACACACAC=0.000, ACACACACACACACACAC=0.000, ACACACACACACACACACAC=0.000, ACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACACACACACACAC=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	374	ACACACACACACACACACACACAC=1.000	ACACACACACAC=0.000, ACACACACACACAC=0.000, ACACACACACACACAC=0.000, ACACACACACACACACAC=0.000, ACACACACACACACACACAC=0.000, ACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACACACACACACAC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	62	ACACACACACACACACACACACAC=1.00	ACACACACACAC=0.00, ACACACACACACAC=0.00, ACACACACACACACAC=0.00, ACACACACACACACACAC=0.00, ACACACACACACACACACAC=0.00, ACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACACAC=0.00, ACACACACACACACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
Other	Sub	328	ACACACACACACACACACACACAC=0.997	ACACACACACAC=0.000, ACACACACACACAC=0.000, ACACACACACACACAC=0.000, ACACACACACACACACAC=0.000, ACACACACACACACACACAC=0.000, ACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACAC=0.003, ACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACACAC=0.000, ACACACACACACACACACACACACACACACACACACACACAC=0.000	1.0	0.0	0.0	N/A

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	15166	(AC)₁₂=0.95793	del(AC)₆=0.00000, del(AC)₅=0.00000, del(AC)₄=0.00000, del(AC)₃=0.00007, delACAC=0.00284, delAC=0.03514, dupAC=0.00330, dupACAC=0.00000, dup(AC)₃=0.00073, dup(AC)₄=0.00000, dup(AC)₅=0.00000, dup(AC)₉=0.00000
Allele Frequency Aggregator	European	Sub	12718	(AC)₁₂=0.94991	del(AC)₆=0.00000, del(AC)₅=0.00000, del(AC)₄=0.00000, del(AC)₃=0.00008, delACAC=0.00338, delAC=0.04191, dupAC=0.00393, dupACAC=0.00000, dup(AC)₃=0.00079, dup(AC)₄=0.00000, dup(AC)₅=0.00000, dup(AC)₉=0.00000
Allele Frequency Aggregator	African	Sub	1550	(AC)₁₂=1.0000	del(AC)₆=0.0000, del(AC)₅=0.0000, del(AC)₄=0.0000, del(AC)₃=0.0000, delACAC=0.0000, delAC=0.0000, dupAC=0.0000, dupACAC=0.0000, dup(AC)₃=0.0000, dup(AC)₄=0.0000, dup(AC)₅=0.0000, dup(AC)₉=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	374	(AC)₁₂=1.000	del(AC)₆=0.000, del(AC)₅=0.000, del(AC)₄=0.000, del(AC)₃=0.000, delACAC=0.000, delAC=0.000, dupAC=0.000, dupACAC=0.000, dup(AC)₃=0.000, dup(AC)₄=0.000, dup(AC)₅=0.000, dup(AC)₉=0.000
Allele Frequency Aggregator	Other	Sub	328	(AC)₁₂=0.997	del(AC)₆=0.000, del(AC)₅=0.000, del(AC)₄=0.000, del(AC)₃=0.000, delACAC=0.000, delAC=0.000, dupAC=0.000, dupACAC=0.000, dup(AC)₃=0.003, dup(AC)₄=0.000, dup(AC)₅=0.000, dup(AC)₉=0.000
Allele Frequency Aggregator	Latin American 1	Sub	110	(AC)₁₂=1.000	del(AC)₆=0.000, del(AC)₅=0.000, del(AC)₄=0.000, del(AC)₃=0.000, delACAC=0.000, delAC=0.000, dupAC=0.000, dupACAC=0.000, dup(AC)₃=0.000, dup(AC)₄=0.000, dup(AC)₅=0.000, dup(AC)₉=0.000
Allele Frequency Aggregator	South Asian	Sub	62	(AC)₁₂=1.00	del(AC)₆=0.00, del(AC)₅=0.00, del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.00, dupAC=0.00, dupACAC=0.00, dup(AC)₃=0.00, dup(AC)₄=0.00, dup(AC)₅=0.00, dup(AC)₉=0.00
Allele Frequency Aggregator	Asian	Sub	24	(AC)₁₂=1.00	del(AC)₆=0.00, del(AC)₅=0.00, del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.00, dupAC=0.00, dupACAC=0.00, dup(AC)₃=0.00, dup(AC)₄=0.00, dup(AC)₅=0.00, dup(AC)₉=0.00
1000Genomes	Global	Study-wide	5008	(AC)₁₂=0.6927	delAC=0.3073
1000Genomes	African	Sub	1322	(AC)₁₂=0.7602	delAC=0.2398
1000Genomes	East Asian	Sub	1008	(AC)₁₂=0.3244	delAC=0.6756
1000Genomes	Europe	Sub	1006	(AC)₁₂=0.8469	delAC=0.1531
1000Genomes	South Asian	Sub	978	(AC)₁₂=0.749	delAC=0.251
1000Genomes	American	Sub	694	(AC)₁₂=0.795	delAC=0.205
The Danish reference pan genome	Danish	Study-wide	40	(AC)₁₂=0.70	delAC=0.30

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 6	NC_000006.12:g.170286803AC[6]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[7]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[8]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[9]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[10]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[11]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[13]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[14]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[15]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[16]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[17]
GRCh38.p14 chr 6	NC_000006.12:g.170286803AC[21]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[6]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[7]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[8]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[9]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[10]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[11]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[13]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[14]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[15]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[16]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[17]
GRCh37.p13 chr 6	NC_000006.11:g.170595891AC[21]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[6]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[7]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[8]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[9]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[10]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[11]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[13]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[14]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[15]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[16]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[17]
DLL1 RefSeqGene	NG_027940.1:g.8784GT[21]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[6]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[7]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[8]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[9]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[10]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[11]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[13]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[14]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[15]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[16]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[17]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041AC[21]

Gene: DLL1, delta like canonical Notch ligand 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DLL1 transcript	NM_005618.4:c.671-528GT[6]	N/A	Intron Variant
DLL1 transcript variant X1	XM_005266934.5:c.671-528G… XM_005266934.5:c.671-528GT[6]	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	(AC)₁₂=	del(AC)₆	del(AC)₅	del(AC)₄	del(AC)₃	delACAC	delAC	dupAC	dupACAC	dup(AC)₃	dup(AC)₄	dup(AC)₅	dup(AC)₉
GRCh38.p14 chr 6	NC_000006.12:g.170286803_170286826=	NC_000006.12:g.170286803AC[6]	NC_000006.12:g.170286803AC[7]	NC_000006.12:g.170286803AC[8]	NC_000006.12:g.170286803AC[9]	NC_000006.12:g.170286803AC[10]	NC_000006.12:g.170286803AC[11]	NC_000006.12:g.170286803AC[13]	NC_000006.12:g.170286803AC[14]	NC_000006.12:g.170286803AC[15]	NC_000006.12:g.170286803AC[16]	NC_000006.12:g.170286803AC[17]	NC_000006.12:g.170286803AC[21]
GRCh37.p13 chr 6	NC_000006.11:g.170595891_170595914=	NC_000006.11:g.170595891AC[6]	NC_000006.11:g.170595891AC[7]	NC_000006.11:g.170595891AC[8]	NC_000006.11:g.170595891AC[9]	NC_000006.11:g.170595891AC[10]	NC_000006.11:g.170595891AC[11]	NC_000006.11:g.170595891AC[13]	NC_000006.11:g.170595891AC[14]	NC_000006.11:g.170595891AC[15]	NC_000006.11:g.170595891AC[16]	NC_000006.11:g.170595891AC[17]	NC_000006.11:g.170595891AC[21]
DLL1 RefSeqGene	NG_027940.1:g.8784_8807=	NG_027940.1:g.8784GT[6]	NG_027940.1:g.8784GT[7]	NG_027940.1:g.8784GT[8]	NG_027940.1:g.8784GT[9]	NG_027940.1:g.8784GT[10]	NG_027940.1:g.8784GT[11]	NG_027940.1:g.8784GT[13]	NG_027940.1:g.8784GT[14]	NG_027940.1:g.8784GT[15]	NG_027940.1:g.8784GT[16]	NG_027940.1:g.8784GT[17]	NG_027940.1:g.8784GT[21]
GRCh38.p14 chr 6 alt locus HSCHR6_1_CTG5	NT_187553.1:g.14041_14064=	NT_187553.1:g.14041AC[6]	NT_187553.1:g.14041AC[7]	NT_187553.1:g.14041AC[8]	NT_187553.1:g.14041AC[9]	NT_187553.1:g.14041AC[10]	NT_187553.1:g.14041AC[11]	NT_187553.1:g.14041AC[13]	NT_187553.1:g.14041AC[14]	NT_187553.1:g.14041AC[15]	NT_187553.1:g.14041AC[16]	NT_187553.1:g.14041AC[17]	NT_187553.1:g.14041AC[21]
DLL1 transcript	NM_005618.3:c.671-505=	NM_005618.3:c.671-528GT[6]	NM_005618.3:c.671-528GT[7]	NM_005618.3:c.671-528GT[8]	NM_005618.3:c.671-528GT[9]	NM_005618.3:c.671-528GT[10]	NM_005618.3:c.671-528GT[11]	NM_005618.3:c.671-528GT[13]	NM_005618.3:c.671-528GT[14]	NM_005618.3:c.671-528GT[15]	NM_005618.3:c.671-528GT[16]	NM_005618.3:c.671-528GT[17]	NM_005618.3:c.671-528GT[21]
DLL1 transcript	NM_005618.4:c.671-505=	NM_005618.4:c.671-528GT[6]	NM_005618.4:c.671-528GT[7]	NM_005618.4:c.671-528GT[8]	NM_005618.4:c.671-528GT[9]	NM_005618.4:c.671-528GT[10]	NM_005618.4:c.671-528GT[11]	NM_005618.4:c.671-528GT[13]	NM_005618.4:c.671-528GT[14]	NM_005618.4:c.671-528GT[15]	NM_005618.4:c.671-528GT[16]	NM_005618.4:c.671-528GT[17]	NM_005618.4:c.671-528GT[21]
DLL1 transcript variant X1	XM_005266934.1:c.671-505=	XM_005266934.1:c.671-528GT[6]	XM_005266934.1:c.671-528GT[7]	XM_005266934.1:c.671-528GT[8]	XM_005266934.1:c.671-528GT[9]	XM_005266934.1:c.671-528GT[10]	XM_005266934.1:c.671-528GT[11]	XM_005266934.1:c.671-528GT[13]	XM_005266934.1:c.671-528GT[14]	XM_005266934.1:c.671-528GT[15]	XM_005266934.1:c.671-528GT[16]	XM_005266934.1:c.671-528GT[17]	XM_005266934.1:c.671-528GT[21]
DLL1 transcript variant X1	XM_005266934.5:c.671-505=	XM_005266934.5:c.671-528GT[6]	XM_005266934.5:c.671-528GT[7]	XM_005266934.5:c.671-528GT[8]	XM_005266934.5:c.671-528GT[9]	XM_005266934.5:c.671-528GT[10]	XM_005266934.5:c.671-528GT[11]	XM_005266934.5:c.671-528GT[13]	XM_005266934.5:c.671-528GT[14]	XM_005266934.5:c.671-528GT[15]	XM_005266934.5:c.671-528GT[16]	XM_005266934.5:c.671-528GT[17]	XM_005266934.5:c.671-528GT[21]

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#.

61 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss326893592	May 09, 2011 (134)
2	1000GENOMES	ss326944497	May 09, 2011 (134)
3	1000GENOMES	ss327217861	Jan 10, 2018 (151)
4	LUNTER	ss551694895	Apr 25, 2013 (138)
5	SSMP	ss663677189	Apr 01, 2015 (144)
6	1000GENOMES	ss1376619844	Aug 21, 2014 (142)
7	EVA_GENOME_DK	ss1576914231	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1705481226	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1705481389	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710307959	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710307960	Apr 01, 2015 (144)
12	SWEGEN	ss3000428301	Nov 08, 2017 (151)
13	MCHAISSO	ss3064238284	Jan 10, 2018 (151)
14	EVA_DECODE	ss3718866532	Jul 13, 2019 (153)
15	EVA_DECODE	ss3718866533	Jul 13, 2019 (153)
16	EVA_DECODE	ss3718866534	Jul 13, 2019 (153)
17	EVA_DECODE	ss3718866535	Jul 13, 2019 (153)
18	EVA_DECODE	ss3718866536	Jul 13, 2019 (153)
19	ACPOP	ss3734249073	Jul 13, 2019 (153)
20	ACPOP	ss3734249074	Jul 13, 2019 (153)
21	ACPOP	ss3734249075	Jul 13, 2019 (153)
22	ACPOP	ss3734249076	Jul 13, 2019 (153)
23	KHV_HUMAN_GENOMES	ss3809207173	Jul 13, 2019 (153)
24	EVA	ss3830349436	Apr 26, 2020 (154)
25	VINODS	ss4025300453	Apr 26, 2021 (155)
26	GNOMAD	ss4156459754	Apr 26, 2021 (155)
27	GNOMAD	ss4156459755	Apr 26, 2021 (155)
28	GNOMAD	ss4156459756	Apr 26, 2021 (155)
29	GNOMAD	ss4156459757	Apr 26, 2021 (155)
30	GNOMAD	ss4156459758	Apr 26, 2021 (155)
31	GNOMAD	ss4156459759	Apr 26, 2021 (155)
32	GNOMAD	ss4156459760	Apr 26, 2021 (155)
33	GNOMAD	ss4156459761	Apr 26, 2021 (155)
34	GNOMAD	ss4156459762	Apr 26, 2021 (155)
35	GNOMAD	ss4156459763	Apr 26, 2021 (155)
36	TOPMED	ss4731763661	Apr 26, 2021 (155)
37	TOPMED	ss4731763662	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5181263357	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5181263358	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5181263359	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5181263360	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5181263361	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5181263362	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5271399529	Oct 13, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5271399530	Oct 13, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5271399531	Oct 13, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5271399532	Oct 13, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5271399533	Oct 13, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5271399534	Oct 13, 2022 (156)
50	HUGCELL_USP	ss5468741885	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5468741886	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5468741887	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5468741888	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5468741889	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5468741890	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5720549799	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5720549800	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5720549801	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5720549802	Oct 13, 2022 (156)
60	TOMMO_GENOMICS	ss5720549803	Oct 13, 2022 (156)
61	EVA	ss5855712828	Oct 13, 2022 (156)
62	1000Genomes	NC_000006.11 - 170595891	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 19728912 (NC_000006.11:170595890:AC: 667/3854) Row 19728913 (NC_000006.11:170595890::AC 82/3854)	-	Oct 12, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 19728912 (NC_000006.11:170595890:AC: 667/3854) Row 19728913 (NC_000006.11:170595890::AC 82/3854)	-	Oct 12, 2018 (152)
65	The Danish reference pan genome	NC_000006.11 - 170595891	Apr 26, 2020 (154)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 249565810 (NC_000006.12:170286802::AC 8090/137252) Row 249565811 (NC_000006.12:170286802::ACAC 190/137332) Row 249565812 (NC_000006.12:170286802::ACACAC 198/137332)...	-	Apr 26, 2021 (155)
76	Northern Sweden Submission ignored due to conflicting rows: Row 7533938 (NC_000006.11:170595890:AC: 28/600) Row 7533939 (NC_000006.11:170595890:ACAC: 20/600) Row 7533940 (NC_000006.11:170595890::AC 10/600)...	-	Jul 13, 2019 (153)
77	Northern Sweden Submission ignored due to conflicting rows: Row 7533938 (NC_000006.11:170595890:AC: 28/600) Row 7533939 (NC_000006.11:170595890:ACAC: 20/600) Row 7533940 (NC_000006.11:170595890::AC 10/600)...	-	Jul 13, 2019 (153)
78	Northern Sweden Submission ignored due to conflicting rows: Row 7533938 (NC_000006.11:170595890:AC: 28/600) Row 7533939 (NC_000006.11:170595890:ACAC: 20/600) Row 7533940 (NC_000006.11:170595890::AC 10/600)...	-	Jul 13, 2019 (153)
79	Northern Sweden Submission ignored due to conflicting rows: Row 7533938 (NC_000006.11:170595890:AC: 28/600) Row 7533939 (NC_000006.11:170595890:ACAC: 20/600) Row 7533940 (NC_000006.11:170595890::AC 10/600)...	-	Jul 13, 2019 (153)
80	8.3KJPN Submission ignored due to conflicting rows: Row 39232664 (NC_000006.11:170595890:AC: 11498/16750) Row 39232665 (NC_000006.11:170595890:ACACAC: 80/16750) Row 39232666 (NC_000006.11:170595890:ACAC: 41/16750)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 39232664 (NC_000006.11:170595890:AC: 11498/16750) Row 39232665 (NC_000006.11:170595890:ACACAC: 80/16750) Row 39232666 (NC_000006.11:170595890:ACAC: 41/16750)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 39232664 (NC_000006.11:170595890:AC: 11498/16750) Row 39232665 (NC_000006.11:170595890:ACACAC: 80/16750) Row 39232666 (NC_000006.11:170595890:ACAC: 41/16750)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 39232664 (NC_000006.11:170595890:AC: 11498/16750) Row 39232665 (NC_000006.11:170595890:ACACAC: 80/16750) Row 39232666 (NC_000006.11:170595890:ACAC: 41/16750)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 39232664 (NC_000006.11:170595890:AC: 11498/16750) Row 39232665 (NC_000006.11:170595890:ACACAC: 80/16750) Row 39232666 (NC_000006.11:170595890:ACAC: 41/16750)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 39232664 (NC_000006.11:170595890:AC: 11498/16750) Row 39232665 (NC_000006.11:170595890:ACACAC: 80/16750) Row 39232666 (NC_000006.11:170595890:ACAC: 41/16750)...	-	Apr 26, 2021 (155)
86	14KJPN Submission ignored due to conflicting rows: Row 54386903 (NC_000006.12:170286802:AC: 19436/28250) Row 54386904 (NC_000006.12:170286802:ACACAC: 136/28250) Row 54386905 (NC_000006.12:170286802:ACAC: 66/28250)...	-	Oct 13, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 54386903 (NC_000006.12:170286802:AC: 19436/28250) Row 54386904 (NC_000006.12:170286802:ACACAC: 136/28250) Row 54386905 (NC_000006.12:170286802:ACAC: 66/28250)...	-	Oct 13, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 54386903 (NC_000006.12:170286802:AC: 19436/28250) Row 54386904 (NC_000006.12:170286802:ACACAC: 136/28250) Row 54386905 (NC_000006.12:170286802:ACAC: 66/28250)...	-	Oct 13, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 54386903 (NC_000006.12:170286802:AC: 19436/28250) Row 54386904 (NC_000006.12:170286802:ACACAC: 136/28250) Row 54386905 (NC_000006.12:170286802:ACAC: 66/28250)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 54386903 (NC_000006.12:170286802:AC: 19436/28250) Row 54386904 (NC_000006.12:170286802:ACACAC: 136/28250) Row 54386905 (NC_000006.12:170286802:ACAC: 66/28250)...	-	Oct 13, 2022 (156)
91	TopMed Submission ignored due to conflicting rows: Row 569141219 (NC_000006.12:170286802::AC 16376/264690) Row 569141220 (NC_000006.12:170286802:ACACACAC: 13/264690)	-	Apr 26, 2021 (155)
92	TopMed Submission ignored due to conflicting rows: Row 569141219 (NC_000006.12:170286802::AC 16376/264690) Row 569141220 (NC_000006.12:170286802:ACACACAC: 13/264690)	-	Apr 26, 2021 (155)
93	UK 10K study - Twins Submission ignored due to conflicting rows: Row 19728912 (NC_000006.11:170595890:AC: 481/3708) Row 19728913 (NC_000006.11:170595890::AC 56/3708)	-	Oct 12, 2018 (152)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 19728912 (NC_000006.11:170595890:AC: 481/3708) Row 19728913 (NC_000006.11:170595890::AC 56/3708)	-	Oct 12, 2018 (152)
95	ALFA	NC_000006.12 - 170286803	Apr 26, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4156459763	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACAC	(self)
ss5181263362	NC_000006.11:170595890:ACACACACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACAC	(self)
ss4156459762, ss5468741889	NC_000006.12:170286802:ACACACACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACAC	(self)
ss4156459761, ss4731763662	NC_000006.12:170286802:ACACACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACAC	(self)
ss5181263358	NC_000006.11:170595890:ACACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACAC	(self)
ss3718866536, ss4156459760, ss5271399534, ss5720549800	NC_000006.12:170286802:ACACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACAC	(self)
ss3000428301, ss3734249074, ss5181263359	NC_000006.11:170595890:ACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACAC	(self)
ss4156459759, ss5271399532, ss5468741885, ss5720549801	NC_000006.12:170286802:ACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACAC	(self)
ss3718866535	NC_000006.12:170286804:ACAC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACAC	(self)
ss326893592, ss326944497, ss551694895	NC_000006.10:170437815:AC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACAC	(self)
35369023, 1126408, ss663677189, ss1376619844, ss1576914231, ss1705481226, ss1705481389, ss3734249073, ss3830349436, ss5181263357	NC_000006.11:170595890:AC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACAC	(self)
ss3064238284, ss3809207173, ss4156459758, ss5271399529, ss5468741886, ss5720549799, ss5855712828	NC_000006.12:170286802:AC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACAC	(self)
ss3718866534	NC_000006.12:170286806:AC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACAC	(self)
ss4025300453	NT_187553.1:14040:AC:	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACAC	(self)
ss327217861	NC_000006.10:170437815::AC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACAC	(self)
ss3734249075, ss5181263360	NC_000006.11:170595890::AC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACAC	(self)
ss1710307959, ss1710307960	NC_000006.11:170595892::AC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACAC	(self)
ss4156459754, ss4731763661, ss5271399530, ss5468741887, ss5720549802	NC_000006.12:170286802::AC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACAC	(self)
ss3718866533	NC_000006.12:170286808::AC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACAC	(self)
ss5181263361	NC_000006.11:170595890::ACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACAC	(self)
ss4156459755, ss5271399531, ss5468741890, ss5720549803	NC_000006.12:170286802::ACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACAC	(self)
ss3734249076	NC_000006.11:170595890::ACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACAC	(self)
ss4156459756, ss5271399533, ss5468741888	NC_000006.12:170286802::ACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACAC	(self)
ss3718866532	NC_000006.12:170286808::ACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACAC	(self)
ss4156459757	NC_000006.12:170286802::ACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACAC	(self)
7446534694	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACAC	NC_000006.12:170286802:ACACACACACA… NC_000006.12:170286802:ACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACAC	(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 rs143742416

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

rs143742416