Name: rs72177430
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.

rs72177430

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:51966282-51966289 (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(T)₅ / del(T)₄ / delT / dupT / …
del(T)₅ / del(T)₄ / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₆ / dup(T)₈ / ins(T)₉ / ins(T)₁₀ / ins(T)₁₆ / ins(T)₂₃ / ins(T)₂₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₅=0.000008 (2/264690, TOPMED)
dupT=0.06211 (1041/16760, 8.3KJPN)
dupT=0.01691 (269/15906, ALFA) (+ 6 more)
dupT=0.1236 (619/5008, 1000G)
dupT=0.0677 (261/3854, ALSPAC)
dupT=0.0785 (291/3708, TWINSUK)
dupT=0.0595 (109/1832, Korea1K)
dupT=0.075 (75/998, GoNL)
dupT=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF350 : Intron Variant
ZNF350-AS1 : 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	15906	TTTTTTTT=0.98277	TTT=0.00000, TTTT=0.00000, TTTTTTT=0.00000, TTTTTTTTT=0.01691, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00013, TTTTTTTTTTTTTTTT=0.00019, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000	0.967166	0.001006	0.031828	9
European	Sub	13090	TTTTTTTT=0.97907	TTT=0.00000, TTTT=0.00000, TTTTTTT=0.00000, TTTTTTTTT=0.02055, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00015, TTTTTTTTTTTTTTTT=0.00023, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000	0.960098	0.001223	0.038679	6
African	Sub	1648	TTTTTTTT=1.0000	TTT=0.0000, TTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	68	TTTTTTTT=1.00	TTT=0.00, TTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1580	TTTTTTTT=1.0000	TTT=0.0000, TTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	100	TTTTTTTT=1.00	TTT=0.00, TTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	80	TTTTTTTT=1.00	TTT=0.00, TTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTT=1.00	TTT=0.00, TTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	106	TTTTTTTT=1.000	TTT=0.000, TTTT=0.000, TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	526	TTTTTTTT=1.000	TTT=0.000, TTTT=0.000, TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	56	TTTTTTTT=1.00	TTT=0.00, TTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	380	TTTTTTTT=1.000	TTT=0.000, TTTT=0.000, TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₈=0.999992	del(T)₅=0.000008
8.3KJPN	JAPANESE	Study-wide	16760	- No frequency provided	dupT=0.06211
Allele Frequency Aggregator	Total	Global	15906	(T)₈=0.98277	del(T)₅=0.00000, del(T)₄=0.00000, delT=0.00000, dupT=0.01691, dupTT=0.00000, dupTTT=0.00000, dup(T)₈=0.00019, ins(T)₂₃=0.00013
Allele Frequency Aggregator	European	Sub	13090	(T)₈=0.97907	del(T)₅=0.00000, del(T)₄=0.00000, delT=0.00000, dupT=0.02055, dupTT=0.00000, dupTTT=0.00000, dup(T)₈=0.00023, ins(T)₂₃=0.00015
Allele Frequency Aggregator	African	Sub	1648	(T)₈=1.0000	del(T)₅=0.0000, del(T)₄=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₈=0.0000, ins(T)₂₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	526	(T)₈=1.000	del(T)₅=0.000, del(T)₄=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₈=0.000, ins(T)₂₃=0.000
Allele Frequency Aggregator	Other	Sub	380	(T)₈=1.000	del(T)₅=0.000, del(T)₄=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₈=0.000, ins(T)₂₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	106	(T)₈=1.000	del(T)₅=0.000, del(T)₄=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₈=0.000, ins(T)₂₃=0.000
Allele Frequency Aggregator	Asian	Sub	100	(T)₈=1.00	del(T)₅=0.00, del(T)₄=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₈=0.00, ins(T)₂₃=0.00
Allele Frequency Aggregator	South Asian	Sub	56	(T)₈=1.00	del(T)₅=0.00, del(T)₄=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₈=0.00, ins(T)₂₃=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.1236
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.1248
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.0694
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.0636
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.278
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.069
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.0677
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.0785
Korean Genome Project	KOREAN	Study-wide	1832	- No frequency provided	dupT=0.0595
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupT=0.075
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.07

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.51966285_51966289del
GRCh38.p14 chr 19	NC_000019.10:g.51966286_51966289del
GRCh38.p14 chr 19	NC_000019.10:g.51966289del
GRCh38.p14 chr 19	NC_000019.10:g.51966289dup
GRCh38.p14 chr 19	NC_000019.10:g.51966288_51966289dup
GRCh38.p14 chr 19	NC_000019.10:g.51966287_51966289dup
GRCh38.p14 chr 19	NC_000019.10:g.51966286_51966289dup
GRCh38.p14 chr 19	NC_000019.10:g.51966284_51966289dup
GRCh38.p14 chr 19	NC_000019.10:g.51966282_51966289dup
GRCh38.p14 chr 19	NC_000019.10:g.51966289_51966290insTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.51966289_51966290insTTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.51966289_51966290insTTTTTTTTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.51966289_51966290insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.51966289_51966290insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.52469538_52469542del
GRCh37.p13 chr 19	NC_000019.9:g.52469539_52469542del
GRCh37.p13 chr 19	NC_000019.9:g.52469542del
GRCh37.p13 chr 19	NC_000019.9:g.52469542dup
GRCh37.p13 chr 19	NC_000019.9:g.52469541_52469542dup
GRCh37.p13 chr 19	NC_000019.9:g.52469540_52469542dup
GRCh37.p13 chr 19	NC_000019.9:g.52469539_52469542dup
GRCh37.p13 chr 19	NC_000019.9:g.52469537_52469542dup
GRCh37.p13 chr 19	NC_000019.9:g.52469535_52469542dup
GRCh37.p13 chr 19	NC_000019.9:g.52469542_52469543insTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.52469542_52469543insTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.52469542_52469543insTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.52469542_52469543insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.52469542_52469543insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: ZNF350, zinc finger protein 350 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF350 transcript	NM_021632.4:c.239-72_239-… NM_021632.4:c.239-72_239-68del	N/A	Intron Variant
ZNF350 transcript variant X1	XM_017027094.2:c.365-72_3… XM_017027094.2:c.365-72_365-68del	N/A	Intron Variant
ZNF350 transcript variant X4	XM_017027096.2:c.365-72_3… XM_017027096.2:c.365-72_365-68del	N/A	Intron Variant
ZNF350 transcript variant X6	XM_017027098.2:c.239-72_2… XM_017027098.2:c.239-72_239-68del	N/A	Intron Variant
ZNF350 transcript variant X8	XM_017027099.2:c.239-72_2… XM_017027099.2:c.239-72_239-68del	N/A	Intron Variant
ZNF350 transcript variant X9	XM_017027100.1:c.239-72_2… XM_017027100.1:c.239-72_239-68del	N/A	Intron Variant
ZNF350 transcript variant X2	XM_047439182.1:c.365-72_3… XM_047439182.1:c.365-72_365-68del	N/A	Intron Variant
ZNF350 transcript variant X3	XM_047439183.1:c.365-72_3… XM_047439183.1:c.365-72_365-68del	N/A	Intron Variant
ZNF350 transcript variant X5	XM_047439184.1:c.239-72_2… XM_047439184.1:c.239-72_239-68del	N/A	Intron Variant
ZNF350 transcript variant X7	XM_047439185.1:c.239-72_2… XM_047439185.1:c.239-72_239-68del	N/A	Intron Variant
ZNF350 transcript variant X10	XM_047439186.1:c.-440-72_… XM_047439186.1:c.-440-72_-440-68del	N/A	Intron Variant
ZNF350 transcript variant X11	XM_047439187.1:c.-440-72_… XM_047439187.1:c.-440-72_-440-68del	N/A	Intron Variant
ZNF350 transcript variant X12	XM_047439188.1:c.-440-72_… XM_047439188.1:c.-440-72_-440-68del	N/A	Intron Variant

Gene: ZNF350-AS1, ZNF350 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF350-AS1 transcript	NR_103847.1:n.	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	(T)₈=	del(T)₅	del(T)₄	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₆	dup(T)₈	ins(T)₉	ins(T)₁₀	ins(T)₁₆	ins(T)₂₃	ins(T)₂₈
GRCh38.p14 chr 19	NC_000019.10:g.51966282_51966289=	NC_000019.10:g.51966285_51966289del	NC_000019.10:g.51966286_51966289del	NC_000019.10:g.51966289del	NC_000019.10:g.51966289dup	NC_000019.10:g.51966288_51966289dup	NC_000019.10:g.51966287_51966289dup	NC_000019.10:g.51966286_51966289dup	NC_000019.10:g.51966284_51966289dup	NC_000019.10:g.51966282_51966289dup	NC_000019.10:g.51966289_51966290insTTTTTTTTT	NC_000019.10:g.51966289_51966290insTTTTTTTTTT	NC_000019.10:g.51966289_51966290insTTTTTTTTTTTTTTTT	NC_000019.10:g.51966289_51966290insTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:g.51966289_51966290insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.52469535_52469542=	NC_000019.9:g.52469538_52469542del	NC_000019.9:g.52469539_52469542del	NC_000019.9:g.52469542del	NC_000019.9:g.52469542dup	NC_000019.9:g.52469541_52469542dup	NC_000019.9:g.52469540_52469542dup	NC_000019.9:g.52469539_52469542dup	NC_000019.9:g.52469537_52469542dup	NC_000019.9:g.52469535_52469542dup	NC_000019.9:g.52469542_52469543insTTTTTTTTT	NC_000019.9:g.52469542_52469543insTTTTTTTTTT	NC_000019.9:g.52469542_52469543insTTTTTTTTTTTTTTTT	NC_000019.9:g.52469542_52469543insTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.9:g.52469542_52469543insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ZNF350 transcript	NM_021632.3:c.239-68=	NM_021632.3:c.239-72_239-68del	NM_021632.3:c.239-71_239-68del	NM_021632.3:c.239-68del	NM_021632.3:c.239-68dup	NM_021632.3:c.239-69_239-68dup	NM_021632.3:c.239-70_239-68dup	NM_021632.3:c.239-71_239-68dup	NM_021632.3:c.239-73_239-68dup	NM_021632.3:c.239-75_239-68dup	NM_021632.3:c.239-68_239-67insAAAAAAAAA	NM_021632.3:c.239-68_239-67insAAAAAAAAAA	NM_021632.3:c.239-68_239-67insAAAAAAAAAAAAAAAA	NM_021632.3:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAA	NM_021632.3:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript	NM_021632.4:c.239-68=	NM_021632.4:c.239-72_239-68del	NM_021632.4:c.239-71_239-68del	NM_021632.4:c.239-68del	NM_021632.4:c.239-68dup	NM_021632.4:c.239-69_239-68dup	NM_021632.4:c.239-70_239-68dup	NM_021632.4:c.239-71_239-68dup	NM_021632.4:c.239-73_239-68dup	NM_021632.4:c.239-75_239-68dup	NM_021632.4:c.239-68_239-67insAAAAAAAAA	NM_021632.4:c.239-68_239-67insAAAAAAAAAA	NM_021632.4:c.239-68_239-67insAAAAAAAAAAAAAAAA	NM_021632.4:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAA	NM_021632.4:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X1	XM_017027094.2:c.365-68=	XM_017027094.2:c.365-72_365-68del	XM_017027094.2:c.365-71_365-68del	XM_017027094.2:c.365-68del	XM_017027094.2:c.365-68dup	XM_017027094.2:c.365-69_365-68dup	XM_017027094.2:c.365-70_365-68dup	XM_017027094.2:c.365-71_365-68dup	XM_017027094.2:c.365-73_365-68dup	XM_017027094.2:c.365-75_365-68dup	XM_017027094.2:c.365-68_365-67insAAAAAAAAA	XM_017027094.2:c.365-68_365-67insAAAAAAAAAA	XM_017027094.2:c.365-68_365-67insAAAAAAAAAAAAAAAA	XM_017027094.2:c.365-68_365-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_017027094.2:c.365-68_365-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X4	XM_017027096.2:c.365-68=	XM_017027096.2:c.365-72_365-68del	XM_017027096.2:c.365-71_365-68del	XM_017027096.2:c.365-68del	XM_017027096.2:c.365-68dup	XM_017027096.2:c.365-69_365-68dup	XM_017027096.2:c.365-70_365-68dup	XM_017027096.2:c.365-71_365-68dup	XM_017027096.2:c.365-73_365-68dup	XM_017027096.2:c.365-75_365-68dup	XM_017027096.2:c.365-68_365-67insAAAAAAAAA	XM_017027096.2:c.365-68_365-67insAAAAAAAAAA	XM_017027096.2:c.365-68_365-67insAAAAAAAAAAAAAAAA	XM_017027096.2:c.365-68_365-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_017027096.2:c.365-68_365-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X6	XM_017027098.2:c.239-68=	XM_017027098.2:c.239-72_239-68del	XM_017027098.2:c.239-71_239-68del	XM_017027098.2:c.239-68del	XM_017027098.2:c.239-68dup	XM_017027098.2:c.239-69_239-68dup	XM_017027098.2:c.239-70_239-68dup	XM_017027098.2:c.239-71_239-68dup	XM_017027098.2:c.239-73_239-68dup	XM_017027098.2:c.239-75_239-68dup	XM_017027098.2:c.239-68_239-67insAAAAAAAAA	XM_017027098.2:c.239-68_239-67insAAAAAAAAAA	XM_017027098.2:c.239-68_239-67insAAAAAAAAAAAAAAAA	XM_017027098.2:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_017027098.2:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X8	XM_017027099.2:c.239-68=	XM_017027099.2:c.239-72_239-68del	XM_017027099.2:c.239-71_239-68del	XM_017027099.2:c.239-68del	XM_017027099.2:c.239-68dup	XM_017027099.2:c.239-69_239-68dup	XM_017027099.2:c.239-70_239-68dup	XM_017027099.2:c.239-71_239-68dup	XM_017027099.2:c.239-73_239-68dup	XM_017027099.2:c.239-75_239-68dup	XM_017027099.2:c.239-68_239-67insAAAAAAAAA	XM_017027099.2:c.239-68_239-67insAAAAAAAAAA	XM_017027099.2:c.239-68_239-67insAAAAAAAAAAAAAAAA	XM_017027099.2:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_017027099.2:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X9	XM_017027100.1:c.239-68=	XM_017027100.1:c.239-72_239-68del	XM_017027100.1:c.239-71_239-68del	XM_017027100.1:c.239-68del	XM_017027100.1:c.239-68dup	XM_017027100.1:c.239-69_239-68dup	XM_017027100.1:c.239-70_239-68dup	XM_017027100.1:c.239-71_239-68dup	XM_017027100.1:c.239-73_239-68dup	XM_017027100.1:c.239-75_239-68dup	XM_017027100.1:c.239-68_239-67insAAAAAAAAA	XM_017027100.1:c.239-68_239-67insAAAAAAAAAA	XM_017027100.1:c.239-68_239-67insAAAAAAAAAAAAAAAA	XM_017027100.1:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_017027100.1:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X2	XM_047439182.1:c.365-68=	XM_047439182.1:c.365-72_365-68del	XM_047439182.1:c.365-71_365-68del	XM_047439182.1:c.365-68del	XM_047439182.1:c.365-68dup	XM_047439182.1:c.365-69_365-68dup	XM_047439182.1:c.365-70_365-68dup	XM_047439182.1:c.365-71_365-68dup	XM_047439182.1:c.365-73_365-68dup	XM_047439182.1:c.365-75_365-68dup	XM_047439182.1:c.365-68_365-67insAAAAAAAAA	XM_047439182.1:c.365-68_365-67insAAAAAAAAAA	XM_047439182.1:c.365-68_365-67insAAAAAAAAAAAAAAAA	XM_047439182.1:c.365-68_365-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_047439182.1:c.365-68_365-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X3	XM_047439183.1:c.365-68=	XM_047439183.1:c.365-72_365-68del	XM_047439183.1:c.365-71_365-68del	XM_047439183.1:c.365-68del	XM_047439183.1:c.365-68dup	XM_047439183.1:c.365-69_365-68dup	XM_047439183.1:c.365-70_365-68dup	XM_047439183.1:c.365-71_365-68dup	XM_047439183.1:c.365-73_365-68dup	XM_047439183.1:c.365-75_365-68dup	XM_047439183.1:c.365-68_365-67insAAAAAAAAA	XM_047439183.1:c.365-68_365-67insAAAAAAAAAA	XM_047439183.1:c.365-68_365-67insAAAAAAAAAAAAAAAA	XM_047439183.1:c.365-68_365-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_047439183.1:c.365-68_365-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X5	XM_047439184.1:c.239-68=	XM_047439184.1:c.239-72_239-68del	XM_047439184.1:c.239-71_239-68del	XM_047439184.1:c.239-68del	XM_047439184.1:c.239-68dup	XM_047439184.1:c.239-69_239-68dup	XM_047439184.1:c.239-70_239-68dup	XM_047439184.1:c.239-71_239-68dup	XM_047439184.1:c.239-73_239-68dup	XM_047439184.1:c.239-75_239-68dup	XM_047439184.1:c.239-68_239-67insAAAAAAAAA	XM_047439184.1:c.239-68_239-67insAAAAAAAAAA	XM_047439184.1:c.239-68_239-67insAAAAAAAAAAAAAAAA	XM_047439184.1:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_047439184.1:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X7	XM_047439185.1:c.239-68=	XM_047439185.1:c.239-72_239-68del	XM_047439185.1:c.239-71_239-68del	XM_047439185.1:c.239-68del	XM_047439185.1:c.239-68dup	XM_047439185.1:c.239-69_239-68dup	XM_047439185.1:c.239-70_239-68dup	XM_047439185.1:c.239-71_239-68dup	XM_047439185.1:c.239-73_239-68dup	XM_047439185.1:c.239-75_239-68dup	XM_047439185.1:c.239-68_239-67insAAAAAAAAA	XM_047439185.1:c.239-68_239-67insAAAAAAAAAA	XM_047439185.1:c.239-68_239-67insAAAAAAAAAAAAAAAA	XM_047439185.1:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_047439185.1:c.239-68_239-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X10	XM_047439186.1:c.-440-68=	XM_047439186.1:c.-440-72_-440-68del	XM_047439186.1:c.-440-71_-440-68del	XM_047439186.1:c.-440-68del	XM_047439186.1:c.-440-68dup	XM_047439186.1:c.-440-69_-440-68dup	XM_047439186.1:c.-440-70_-440-68dup	XM_047439186.1:c.-440-71_-440-68dup	XM_047439186.1:c.-440-73_-440-68dup	XM_047439186.1:c.-440-75_-440-68dup	XM_047439186.1:c.-440-68_-440-67insAAAAAAAAA	XM_047439186.1:c.-440-68_-440-67insAAAAAAAAAA	XM_047439186.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAA	XM_047439186.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_047439186.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X11	XM_047439187.1:c.-440-68=	XM_047439187.1:c.-440-72_-440-68del	XM_047439187.1:c.-440-71_-440-68del	XM_047439187.1:c.-440-68del	XM_047439187.1:c.-440-68dup	XM_047439187.1:c.-440-69_-440-68dup	XM_047439187.1:c.-440-70_-440-68dup	XM_047439187.1:c.-440-71_-440-68dup	XM_047439187.1:c.-440-73_-440-68dup	XM_047439187.1:c.-440-75_-440-68dup	XM_047439187.1:c.-440-68_-440-67insAAAAAAAAA	XM_047439187.1:c.-440-68_-440-67insAAAAAAAAAA	XM_047439187.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAA	XM_047439187.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_047439187.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF350 transcript variant X12	XM_047439188.1:c.-440-68=	XM_047439188.1:c.-440-72_-440-68del	XM_047439188.1:c.-440-71_-440-68del	XM_047439188.1:c.-440-68del	XM_047439188.1:c.-440-68dup	XM_047439188.1:c.-440-69_-440-68dup	XM_047439188.1:c.-440-70_-440-68dup	XM_047439188.1:c.-440-71_-440-68dup	XM_047439188.1:c.-440-73_-440-68dup	XM_047439188.1:c.-440-75_-440-68dup	XM_047439188.1:c.-440-68_-440-67insAAAAAAAAA	XM_047439188.1:c.-440-68_-440-67insAAAAAAAAAA	XM_047439188.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAA	XM_047439188.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAAAAAAAAA	XM_047439188.1:c.-440-68_-440-67insAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

54 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss328281214	May 09, 2011 (138)
2	1000GENOMES	ss499607391	May 04, 2012 (138)
3	LUNTER	ss552634310	Apr 25, 2013 (138)
4	LUNTER	ss553023975	Apr 25, 2013 (138)
5	SSMP	ss664451326	Apr 01, 2015 (144)
6	SSIP	ss947397092	Aug 21, 2014 (142)
7	EVA-GONL	ss994395086	Aug 21, 2014 (142)
8	1000GENOMES	ss1378245708	Aug 21, 2014 (142)
9	EVA_GENOME_DK	ss1575309310	Apr 01, 2015 (144)
10	EVA_DECODE	ss1698449706	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1709241732	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1709241921	Apr 01, 2015 (144)
13	JJLAB	ss2031412537	Sep 14, 2016 (149)
14	SWEGEN	ss3017638303	Nov 08, 2017 (151)
15	BEROUKHIMLAB	ss3644439893	Oct 12, 2018 (152)
16	EVA_DECODE	ss3702960437	Jul 13, 2019 (153)
17	ACPOP	ss3743122790	Jul 13, 2019 (153)
18	ACPOP	ss3743122791	Jul 13, 2019 (153)
19	PACBIO	ss3788558824	Jul 13, 2019 (153)
20	PACBIO	ss3793464322	Jul 13, 2019 (153)
21	PACBIO	ss3798351270	Jul 13, 2019 (153)
22	KHV_HUMAN_GENOMES	ss3821426906	Jul 13, 2019 (153)
23	EVA	ss3835511720	Apr 27, 2020 (154)
24	KOGIC	ss3981571173	Apr 27, 2020 (154)
25	FSA-LAB	ss3984161649	Apr 27, 2021 (155)
26	FSA-LAB	ss3984161650	Apr 27, 2021 (155)
27	EVA	ss3986811405	Apr 27, 2021 (155)
28	GNOMAD	ss4332881395	Apr 27, 2021 (155)
29	GNOMAD	ss4332881396	Apr 27, 2021 (155)
30	GNOMAD	ss4332881397	Apr 27, 2021 (155)
31	GNOMAD	ss4332881398	Apr 27, 2021 (155)
32	GNOMAD	ss4332881399	Apr 27, 2021 (155)
33	GNOMAD	ss4332881400	Apr 27, 2021 (155)
34	GNOMAD	ss4332881401	Apr 27, 2021 (155)
35	GNOMAD	ss4332881402	Apr 27, 2021 (155)
36	GNOMAD	ss4332881403	Apr 27, 2021 (155)
37	GNOMAD	ss4332881404	Apr 27, 2021 (155)
38	GNOMAD	ss4332881406	Apr 27, 2021 (155)
39	TOPMED	ss5077962953	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5228225661	Apr 27, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5307603542	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5307603543	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5307603544	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5500067879	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5500067880	Oct 13, 2022 (156)
46	EVA	ss5512124153	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5787017542	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5787017543	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5787017544	Oct 13, 2022 (156)
50	YY_MCH	ss5817686344	Oct 13, 2022 (156)
51	EVA	ss5840685480	Oct 13, 2022 (156)
52	EVA	ss5852325892	Oct 13, 2022 (156)
53	EVA	ss5928472869	Oct 13, 2022 (156)
54	EVA	ss5953993849	Oct 13, 2022 (156)
55	1000Genomes	NC_000019.9 - 52469535	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 52469535	Oct 12, 2018 (152)
57	The Danish reference pan genome	NC_000019.9 - 52469535	Apr 27, 2020 (154)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542785768 (NC_000019.10:51966281::T 15953/137608) Row 542785769 (NC_000019.10:51966281::TT 1427/137678) Row 542785770 (NC_000019.10:51966281::TTT 79/137764)...	-	Apr 27, 2021 (155)
69	Genome of the Netherlands Release 5	NC_000019.9 - 52469535	Apr 27, 2020 (154)
70	Korean Genome Project	NC_000019.10 - 51966282	Apr 27, 2020 (154)
71	Northern Sweden Submission ignored due to conflicting rows: Row 16407655 (NC_000019.9:52469534::T 39/600) Row 16407656 (NC_000019.9:52469534::TTTTTTTTT 2/600)	-	Jul 13, 2019 (153)
72	Northern Sweden Submission ignored due to conflicting rows: Row 16407655 (NC_000019.9:52469534::T 39/600) Row 16407656 (NC_000019.9:52469534::TTTTTTTTT 2/600)	-	Jul 13, 2019 (153)
73	8.3KJPN	NC_000019.9 - 52469535	Apr 27, 2021 (155)
74	14KJPN Submission ignored due to conflicting rows: Row 120854646 (NC_000019.10:51966281::T 1636/28256) Row 120854647 (NC_000019.10:51966281::TT 1/28256) Row 120854648 (NC_000019.10:51966281:TTTTT: 1/28256)	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 120854646 (NC_000019.10:51966281::T 1636/28256) Row 120854647 (NC_000019.10:51966281::TT 1/28256) Row 120854648 (NC_000019.10:51966281:TTTTT: 1/28256)	-	Oct 13, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 120854646 (NC_000019.10:51966281::T 1636/28256) Row 120854647 (NC_000019.10:51966281::TT 1/28256) Row 120854648 (NC_000019.10:51966281:TTTTT: 1/28256)	-	Oct 13, 2022 (156)
77	TopMed	NC_000019.10 - 51966282	Apr 27, 2021 (155)
78	UK 10K study - Twins	NC_000019.9 - 52469535	Oct 12, 2018 (152)
79	ALFA	NC_000019.10 - 51966282	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)
rs145562815	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
293508617, ss5077962953, ss5787017544	NC_000019.10:51966281:TTTTT:	NC_000019.10:51966281:TTTTTTTT:TTT	(self)
8495351350	NC_000019.10:51966281:TTTTTTTT:TTT	NC_000019.10:51966281:TTTTTTTT:TTT	(self)
ss4332881406	NC_000019.10:51966281:TTTT:	NC_000019.10:51966281:TTTTTTTT:TTTT	(self)
8495351350	NC_000019.10:51966281:TTTTTTTT:TTTT	NC_000019.10:51966281:TTTTTTTT:TTTT	(self)
ss5512124153	NC_000019.9:52469534:T:	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTT
8495351350	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTT	(self)
ss328281214, ss552634310, ss553023975, ss1698449706	NC_000019.8:57161346::T	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTT	(self)
76964175, 42608667, 640147, 18981041, 86194968, 42608667, ss499607391, ss664451326, ss947397092, ss994395086, ss1378245708, ss1575309310, ss1709241732, ss1709241921, ss2031412537, ss3017638303, ss3644439893, ss3743122790, ss3788558824, ss3793464322, ss3798351270, ss3835511720, ss3984161649, ss3986811405, ss5228225661, ss5840685480, ss5953993849	NC_000019.9:52469534::T	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTT	(self)
ss3984161650	NC_000019.9:52469542::T	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTT	(self)
37949174, ss3702960437, ss3821426906, ss3981571173, ss4332881395, ss5307603542, ss5500067879, ss5787017542, ss5817686344, ss5852325892, ss5928472869	NC_000019.10:51966281::T	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTT	(self)
8495351350	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTT	(self)
ss4332881396, ss5307603543, ss5500067880, ss5787017543	NC_000019.10:51966281::TT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTT	(self)
8495351350	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTT	(self)
ss4332881397, ss5307603544	NC_000019.10:51966281::TTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTT	(self)
8495351350	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTT	(self)
ss4332881398	NC_000019.10:51966281::TTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTT	(self)
ss4332881399	NC_000019.10:51966281::TTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4332881400	NC_000019.10:51966281::TTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTT	(self)
8495351350	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3743122791	NC_000019.9:52469534::TTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4332881401	NC_000019.10:51966281::TTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4332881402	NC_000019.10:51966281::TTTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4332881403	NC_000019.10:51966281::TTTTTTTTTTT… NC_000019.10:51966281::TTTTTTTTTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
8495351350	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332881404	NC_000019.10:51966281::TTTTTTTTTTT… NC_000019.10:51966281::TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:51966281:TTTTTTTT:TTT… NC_000019.10:51966281:TTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs72177430

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

rs72177430