Name: rs35544795
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.

rs35544795

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:122071194-122071220 (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(GT)₉ / del(GT)₈ / del(GT)₆ / d…
del(GT)₉ / del(GT)₈ / del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅
Variation Type: Indel Insertion and Deletion
Frequency: delGT=0.1836 (1399/7620, ALFA)
(TG)₁₃T=0.0507 (58/1144, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SRFBP1 : Intron Variant
LOX : 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	7620	TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.7155	TGTGTGTGT=0.0000, TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0031, TGTGTGTGTGTGTGTGTGTGTGT=0.0934, TGTGTGTGTGTGTGTGTGTGTGTGT=0.1836, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0026, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0017, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.701839	0.073249	0.224911	32
European	Sub	6800	TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.6821	TGTGTGTGT=0.0000, TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0035, TGTGTGTGTGTGTGTGTGTGTGT=0.1041, TGTGTGTGTGTGTGTGTGTGTGTGT=0.2054, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0029, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0019, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.656888	0.084293	0.258819	32
African	Sub	256	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGT=0.0, TGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
African American	Sub	252	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	56	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	38	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	36	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	294	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	34	TGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGT=0.00, TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	144	TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.958	TGTGTGTGT=0.000, TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.028, TGTGTGTGTGTGTGTGTGTGTGTGT=0.014, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=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
Allele Frequency Aggregator	Total	Global	7620	(TG)₁₃T=0.7155	del(GT)₉=0.0000, del(GT)₈=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0031, delGTGT=0.0934, delGT=0.1836, dupGT=0.0026, dupGTGT=0.0017, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000
Allele Frequency Aggregator	European	Sub	6800	(TG)₁₃T=0.6821	del(GT)₉=0.0000, del(GT)₈=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0035, delGTGT=0.1041, delGT=0.2054, dupGT=0.0029, dupGTGT=0.0019, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	294	(TG)₁₃T=1.000	del(GT)₉=0.000, del(GT)₈=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000
Allele Frequency Aggregator	African	Sub	256	(TG)₁₃T=1.000	del(GT)₉=0.000, del(GT)₈=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000
Allele Frequency Aggregator	Other	Sub	144	(TG)₁₃T=0.958	del(GT)₉=0.000, del(GT)₈=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.028, delGT=0.014, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000
Allele Frequency Aggregator	Asian	Sub	56	(TG)₁₃T=1.00	del(GT)₉=0.00, del(GT)₈=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	36	(TG)₁₃T=1.00	del(GT)₉=0.00, del(GT)₈=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	34	(TG)₁₃T=1.00	del(GT)₉=0.00, del(GT)₈=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00
1000Genomes	Global	Study-wide	1144	(TG)₁₃T=0.0507	delGT=0.9493
1000Genomes	African	Sub	455	(TG)₁₃T=0.108	delGT=0.892
1000Genomes	Europe	Sub	255	(TG)₁₃T=0.012	delGT=0.988
1000Genomes	South Asian	Sub	193	(TG)₁₃T=0.026	delGT=0.974
1000Genomes	American	Sub	131	(TG)₁₃T=0.008	delGT=0.992
1000Genomes	East Asian	Sub	110	(TG)₁₃T=0.000	delGT=1.000

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 5	NC_000005.10:g.122071195GT[4]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[5]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[7]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[8]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[9]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[10]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[11]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[12]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[14]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[15]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[16]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[17]
GRCh38.p14 chr 5	NC_000005.10:g.122071195GT[18]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[4]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[5]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[7]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[8]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[9]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[10]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[11]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[12]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[14]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[15]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[16]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[17]
GRCh37.p13 chr 5	NC_000005.9:g.121406890GT[18]
LOX RefSeqGene	NG_008722.1:g.12142CA[4]
LOX RefSeqGene	NG_008722.1:g.12142CA[5]
LOX RefSeqGene	NG_008722.1:g.12142CA[7]
LOX RefSeqGene	NG_008722.1:g.12142CA[8]
LOX RefSeqGene	NG_008722.1:g.12142CA[9]
LOX RefSeqGene	NG_008722.1:g.12142CA[10]
LOX RefSeqGene	NG_008722.1:g.12142CA[11]
LOX RefSeqGene	NG_008722.1:g.12142CA[12]
LOX RefSeqGene	NG_008722.1:g.12142CA[14]
LOX RefSeqGene	NG_008722.1:g.12142CA[15]
LOX RefSeqGene	NG_008722.1:g.12142CA[16]
LOX RefSeqGene	NG_008722.1:g.12142CA[17]
LOX RefSeqGene	NG_008722.1:g.12142CA[18]

Gene: LOX, lysyl oxidase (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOX transcript variant 2	NM_001178102.2:c.346-630C… NM_001178102.2:c.346-630CA[4]	N/A	Intron Variant
LOX transcript variant 3	NM_001317073.1:c.145-630C… NM_001317073.1:c.145-630CA[4]	N/A	Intron Variant
LOX transcript variant 1	NM_002317.7:c.1036-630CA[… NM_002317.7:c.1036-630CA[4]	N/A	Intron Variant

Gene: SRFBP1, serum response factor binding protein 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SRFBP1 transcript	NM_152546.3:c.	N/A	Genic Downstream Transcript Variant
SRFBP1 transcript variant X1	XM_017009111.3:c.1106-412… XM_017009111.3:c.1106-4121TG[4]	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	(TG)₁₃T=	del(GT)₉	del(GT)₈	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅
GRCh38.p14 chr 5	NC_000005.10:g.122071194_122071220=	NC_000005.10:g.122071195GT[4]	NC_000005.10:g.122071195GT[5]	NC_000005.10:g.122071195GT[7]	NC_000005.10:g.122071195GT[8]	NC_000005.10:g.122071195GT[9]	NC_000005.10:g.122071195GT[10]	NC_000005.10:g.122071195GT[11]	NC_000005.10:g.122071195GT[12]	NC_000005.10:g.122071195GT[14]	NC_000005.10:g.122071195GT[15]	NC_000005.10:g.122071195GT[16]	NC_000005.10:g.122071195GT[17]	NC_000005.10:g.122071195GT[18]
GRCh37.p13 chr 5	NC_000005.9:g.121406889_121406915=	NC_000005.9:g.121406890GT[4]	NC_000005.9:g.121406890GT[5]	NC_000005.9:g.121406890GT[7]	NC_000005.9:g.121406890GT[8]	NC_000005.9:g.121406890GT[9]	NC_000005.9:g.121406890GT[10]	NC_000005.9:g.121406890GT[11]	NC_000005.9:g.121406890GT[12]	NC_000005.9:g.121406890GT[14]	NC_000005.9:g.121406890GT[15]	NC_000005.9:g.121406890GT[16]	NC_000005.9:g.121406890GT[17]	NC_000005.9:g.121406890GT[18]
LOX RefSeqGene	NG_008722.1:g.12141_12167=	NG_008722.1:g.12142CA[4]	NG_008722.1:g.12142CA[5]	NG_008722.1:g.12142CA[7]	NG_008722.1:g.12142CA[8]	NG_008722.1:g.12142CA[9]	NG_008722.1:g.12142CA[10]	NG_008722.1:g.12142CA[11]	NG_008722.1:g.12142CA[12]	NG_008722.1:g.12142CA[14]	NG_008722.1:g.12142CA[15]	NG_008722.1:g.12142CA[16]	NG_008722.1:g.12142CA[17]	NG_008722.1:g.12142CA[18]
LOX transcript variant 2	NM_001178102.1:c.346-605=	NM_001178102.1:c.346-630CA[4]	NM_001178102.1:c.346-630CA[5]	NM_001178102.1:c.346-630CA[7]	NM_001178102.1:c.346-630CA[8]	NM_001178102.1:c.346-630CA[9]	NM_001178102.1:c.346-630CA[10]	NM_001178102.1:c.346-630CA[11]	NM_001178102.1:c.346-630CA[12]	NM_001178102.1:c.346-630CA[14]	NM_001178102.1:c.346-630CA[15]	NM_001178102.1:c.346-630CA[16]	NM_001178102.1:c.346-630CA[17]	NM_001178102.1:c.346-630CA[18]
LOX transcript variant 2	NM_001178102.2:c.346-605=	NM_001178102.2:c.346-630CA[4]	NM_001178102.2:c.346-630CA[5]	NM_001178102.2:c.346-630CA[7]	NM_001178102.2:c.346-630CA[8]	NM_001178102.2:c.346-630CA[9]	NM_001178102.2:c.346-630CA[10]	NM_001178102.2:c.346-630CA[11]	NM_001178102.2:c.346-630CA[12]	NM_001178102.2:c.346-630CA[14]	NM_001178102.2:c.346-630CA[15]	NM_001178102.2:c.346-630CA[16]	NM_001178102.2:c.346-630CA[17]	NM_001178102.2:c.346-630CA[18]
LOX transcript variant 3	NM_001317073.1:c.145-605=	NM_001317073.1:c.145-630CA[4]	NM_001317073.1:c.145-630CA[5]	NM_001317073.1:c.145-630CA[7]	NM_001317073.1:c.145-630CA[8]	NM_001317073.1:c.145-630CA[9]	NM_001317073.1:c.145-630CA[10]	NM_001317073.1:c.145-630CA[11]	NM_001317073.1:c.145-630CA[12]	NM_001317073.1:c.145-630CA[14]	NM_001317073.1:c.145-630CA[15]	NM_001317073.1:c.145-630CA[16]	NM_001317073.1:c.145-630CA[17]	NM_001317073.1:c.145-630CA[18]
LOX transcript variant 1	NM_002317.5:c.1036-605=	NM_002317.5:c.1036-630CA[4]	NM_002317.5:c.1036-630CA[5]	NM_002317.5:c.1036-630CA[7]	NM_002317.5:c.1036-630CA[8]	NM_002317.5:c.1036-630CA[9]	NM_002317.5:c.1036-630CA[10]	NM_002317.5:c.1036-630CA[11]	NM_002317.5:c.1036-630CA[12]	NM_002317.5:c.1036-630CA[14]	NM_002317.5:c.1036-630CA[15]	NM_002317.5:c.1036-630CA[16]	NM_002317.5:c.1036-630CA[17]	NM_002317.5:c.1036-630CA[18]
LOX transcript variant 1	NM_002317.7:c.1036-605=	NM_002317.7:c.1036-630CA[4]	NM_002317.7:c.1036-630CA[5]	NM_002317.7:c.1036-630CA[7]	NM_002317.7:c.1036-630CA[8]	NM_002317.7:c.1036-630CA[9]	NM_002317.7:c.1036-630CA[10]	NM_002317.7:c.1036-630CA[11]	NM_002317.7:c.1036-630CA[12]	NM_002317.7:c.1036-630CA[14]	NM_002317.7:c.1036-630CA[15]	NM_002317.7:c.1036-630CA[16]	NM_002317.7:c.1036-630CA[17]	NM_002317.7:c.1036-630CA[18]
LOX transcript variant X1	XM_005271990.1:c.1036-605=	XM_005271990.1:c.1036-630CA[4]	XM_005271990.1:c.1036-630CA[5]	XM_005271990.1:c.1036-630CA[7]	XM_005271990.1:c.1036-630CA[8]	XM_005271990.1:c.1036-630CA[9]	XM_005271990.1:c.1036-630CA[10]	XM_005271990.1:c.1036-630CA[11]	XM_005271990.1:c.1036-630CA[12]	XM_005271990.1:c.1036-630CA[14]	XM_005271990.1:c.1036-630CA[15]	XM_005271990.1:c.1036-630CA[16]	XM_005271990.1:c.1036-630CA[17]	XM_005271990.1:c.1036-630CA[18]
SRFBP1 transcript variant X1	XM_017009111.3:c.1106-4121=	XM_017009111.3:c.1106-4121TG[4]	XM_017009111.3:c.1106-4121TG[5]	XM_017009111.3:c.1106-4121TG[7]	XM_017009111.3:c.1106-4121TG[8]	XM_017009111.3:c.1106-4121TG[9]	XM_017009111.3:c.1106-4121TG[10]	XM_017009111.3:c.1106-4121TG[11]	XM_017009111.3:c.1106-4121TG[12]	XM_017009111.3:c.1106-4121TG[14]	XM_017009111.3:c.1106-4121TG[15]	XM_017009111.3:c.1106-4121TG[16]	XM_017009111.3:c.1106-4121TG[17]	XM_017009111.3:c.1106-4121TG[18]

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#.

71 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42611398	Oct 12, 2018 (152)
2	HGSV	ss80905124	Dec 15, 2007 (129)
3	HGSV	ss82980569	Jan 10, 2018 (151)
4	GMI	ss288655314	May 04, 2012 (137)
5	PJP	ss295242612	Jan 10, 2018 (151)
6	1000GENOMES	ss326713704	May 09, 2011 (134)
7	1000GENOMES	ss326757518	May 09, 2011 (135)
8	1000GENOMES	ss326981298	May 09, 2011 (135)
9	LUNTER	ss551538821	Apr 25, 2013 (138)
10	LUNTER	ss551705631	Apr 25, 2013 (138)
11	LUNTER	ss553214865	Apr 25, 2013 (138)
12	SSMP	ss663555351	Apr 01, 2015 (144)
13	BILGI_BIOE	ss666326496	Apr 25, 2013 (138)
14	1000GENOMES	ss1374416305	Aug 21, 2014 (142)
15	1000GENOMES	ss1374416306	Aug 21, 2014 (142)
16	HAMMER_LAB	ss1804053855	Sep 08, 2015 (146)
17	SWEGEN	ss2997689454	Nov 08, 2017 (151)
18	MCHAISSO	ss3064173200	Jan 10, 2018 (151)
19	MCHAISSO	ss3065049003	Nov 08, 2017 (151)
20	URBANLAB	ss3648156640	Oct 12, 2018 (152)
21	EVA_DECODE	ss3715575599	Jul 13, 2019 (153)
22	EVA_DECODE	ss3715575600	Jul 13, 2019 (153)
23	EVA_DECODE	ss3715575601	Jul 13, 2019 (153)
24	EVA_DECODE	ss3715575602	Jul 13, 2019 (153)
25	EVA_DECODE	ss3715575603	Jul 13, 2019 (153)
26	ACPOP	ss3732762191	Jul 13, 2019 (153)
27	ACPOP	ss3732762192	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3807156672	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3807156673	Jul 13, 2019 (153)
30	EVA	ss3829473591	Apr 26, 2020 (154)
31	EVA	ss3838211142	Apr 26, 2020 (154)
32	KOGIC	ss3957529807	Apr 26, 2020 (154)
33	KOGIC	ss3957529808	Apr 26, 2020 (154)
34	KOGIC	ss3957529809	Apr 26, 2020 (154)
35	KOGIC	ss3957529810	Apr 26, 2020 (154)
36	KOGIC	ss3957529811	Apr 26, 2020 (154)
37	GNOMAD	ss4128173375	Apr 26, 2021 (155)
38	GNOMAD	ss4128173376	Apr 26, 2021 (155)
39	GNOMAD	ss4128173377	Apr 26, 2021 (155)
40	GNOMAD	ss4128173378	Apr 26, 2021 (155)
41	GNOMAD	ss4128173379	Apr 26, 2021 (155)
42	GNOMAD	ss4128173381	Apr 26, 2021 (155)
43	GNOMAD	ss4128173382	Apr 26, 2021 (155)
44	GNOMAD	ss4128173383	Apr 26, 2021 (155)
45	GNOMAD	ss4128173384	Apr 26, 2021 (155)
46	GNOMAD	ss4128173385	Apr 26, 2021 (155)
47	GNOMAD	ss4128173386	Apr 26, 2021 (155)
48	GNOMAD	ss4128173387	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5173845080	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5173845081	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5173845082	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5173845083	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5173845084	Apr 26, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5265611885	Oct 17, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5265611886	Oct 17, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5265611887	Oct 17, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5265611888	Oct 17, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5265611889	Oct 17, 2022 (156)
59	HUGCELL_USP	ss5463604305	Oct 17, 2022 (156)
60	HUGCELL_USP	ss5463604306	Oct 17, 2022 (156)
61	HUGCELL_USP	ss5463604307	Oct 17, 2022 (156)
62	HUGCELL_USP	ss5463604308	Oct 17, 2022 (156)
63	HUGCELL_USP	ss5463604309	Oct 17, 2022 (156)
64	HUGCELL_USP	ss5463604310	Oct 17, 2022 (156)
65	TOMMO_GENOMICS	ss5710836370	Oct 17, 2022 (156)
66	TOMMO_GENOMICS	ss5710836371	Oct 17, 2022 (156)
67	TOMMO_GENOMICS	ss5710836372	Oct 17, 2022 (156)
68	TOMMO_GENOMICS	ss5710836374	Oct 17, 2022 (156)
69	TOMMO_GENOMICS	ss5710836375	Oct 17, 2022 (156)
70	EVA	ss5835555004	Oct 17, 2022 (156)
71	EVA	ss5835555005	Oct 17, 2022 (156)
72	1000Genomes	NC_000005.9 - 121406889	Oct 12, 2018 (152)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 202445172 (NC_000005.10:122071193::TG 8063/138018) Row 202445173 (NC_000005.10:122071193::TGTG 2835/138060) Row 202445174 (NC_000005.10:122071193::TGTGTG 1319/138064)...	-	Apr 26, 2021 (155)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 13907808 (NC_000005.10:122071195:TGTG: 314/1832) Row 13907809 (NC_000005.10:122071197:TG: 149/1832) Row 13907810 (NC_000005.10:122071199::TG 5/1832)...	-	Apr 26, 2020 (154)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 13907808 (NC_000005.10:122071195:TGTG: 314/1832) Row 13907809 (NC_000005.10:122071197:TG: 149/1832) Row 13907810 (NC_000005.10:122071199::TG 5/1832)...	-	Apr 26, 2020 (154)
87	Korean Genome Project Submission ignored due to conflicting rows: Row 13907808 (NC_000005.10:122071195:TGTG: 314/1832) Row 13907809 (NC_000005.10:122071197:TG: 149/1832) Row 13907810 (NC_000005.10:122071199::TG 5/1832)...	-	Apr 26, 2020 (154)
88	Korean Genome Project Submission ignored due to conflicting rows: Row 13907808 (NC_000005.10:122071195:TGTG: 314/1832) Row 13907809 (NC_000005.10:122071197:TG: 149/1832) Row 13907810 (NC_000005.10:122071199::TG 5/1832)...	-	Apr 26, 2020 (154)
89	Korean Genome Project Submission ignored due to conflicting rows: Row 13907808 (NC_000005.10:122071195:TGTG: 314/1832) Row 13907809 (NC_000005.10:122071197:TG: 149/1832) Row 13907810 (NC_000005.10:122071199::TG 5/1832)...	-	Apr 26, 2020 (154)
90	Northern Sweden Submission ignored due to conflicting rows: Row 6047056 (NC_000005.9:121406888:TG: 230/600) Row 6047057 (NC_000005.9:121406888:TGTG: 67/600)	-	Jul 13, 2019 (153)
91	Northern Sweden Submission ignored due to conflicting rows: Row 6047056 (NC_000005.9:121406888:TG: 230/600) Row 6047057 (NC_000005.9:121406888:TGTG: 67/600)	-	Jul 13, 2019 (153)
92	8.3KJPN Submission ignored due to conflicting rows: Row 31814387 (NC_000005.9:121406888:TGTG: 2235/16760) Row 31814388 (NC_000005.9:121406888:TG: 2001/16760) Row 31814389 (NC_000005.9:121406888:TGTGTG: 7/16760)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 31814387 (NC_000005.9:121406888:TGTG: 2235/16760) Row 31814388 (NC_000005.9:121406888:TG: 2001/16760) Row 31814389 (NC_000005.9:121406888:TGTGTG: 7/16760)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 31814387 (NC_000005.9:121406888:TGTG: 2235/16760) Row 31814388 (NC_000005.9:121406888:TG: 2001/16760) Row 31814389 (NC_000005.9:121406888:TGTGTG: 7/16760)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 31814387 (NC_000005.9:121406888:TGTG: 2235/16760) Row 31814388 (NC_000005.9:121406888:TG: 2001/16760) Row 31814389 (NC_000005.9:121406888:TGTGTG: 7/16760)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 31814387 (NC_000005.9:121406888:TGTG: 2235/16760) Row 31814388 (NC_000005.9:121406888:TG: 2001/16760) Row 31814389 (NC_000005.9:121406888:TGTGTG: 7/16760)...	-	Apr 26, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 44673474 (NC_000005.10:122071193:TGTGTG: 9/28258) Row 44673475 (NC_000005.10:122071193:TGTG: 3759/28258) Row 44673476 (NC_000005.10:122071193:TG: 3411/28258)...	-	Oct 17, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 44673474 (NC_000005.10:122071193:TGTGTG: 9/28258) Row 44673475 (NC_000005.10:122071193:TGTG: 3759/28258) Row 44673476 (NC_000005.10:122071193:TG: 3411/28258)...	-	Oct 17, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 44673474 (NC_000005.10:122071193:TGTGTG: 9/28258) Row 44673475 (NC_000005.10:122071193:TGTG: 3759/28258) Row 44673476 (NC_000005.10:122071193:TG: 3411/28258)...	-	Oct 17, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 44673474 (NC_000005.10:122071193:TGTGTG: 9/28258) Row 44673475 (NC_000005.10:122071193:TGTG: 3759/28258) Row 44673476 (NC_000005.10:122071193:TG: 3411/28258)...	-	Oct 17, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 44673474 (NC_000005.10:122071193:TGTGTG: 9/28258) Row 44673475 (NC_000005.10:122071193:TGTG: 3759/28258) Row 44673476 (NC_000005.10:122071193:TG: 3411/28258)...	-	Oct 17, 2022 (156)
102	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 3531700 (NC_000005.9:121406888:TG: 32/185) Row 3531701 (NC_000005.9:121406888:TGTG: 27/180)	-	Jul 13, 2019 (153)
103	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 3531700 (NC_000005.9:121406888:TG: 32/185) Row 3531701 (NC_000005.9:121406888:TGTG: 27/180)	-	Jul 13, 2019 (153)
104	ALFA	NC_000005.10 - 122071194	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).

Associated ID	History Updated (Build)
rs71672590	May 11, 2012 (137)
rs138727531	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4128173387	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGT	(self)
ss4128173386	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss4128173385	NC_000005.10:122071193:TGTGTGTGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
ss4128173384	NC_000005.10:122071193:TGTGTGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss2997689454, ss5173845082	NC_000005.9:121406888:TGTGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss3715575599, ss3957529810, ss4128173383, ss5463604305, ss5710836370	NC_000005.10:122071193:TGTGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss288655314, ss326713704, ss553214865	NC_000005.8:121434787:TGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss80905124	NC_000005.8:121434810:GTGT:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1804053855, ss3732762192, ss5173845080, ss5835555005	NC_000005.9:121406888:TGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3065049003, ss3807156672, ss4128173382, ss5265611886, ss5463604306, ss5710836371	NC_000005.10:122071193:TGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715575600, ss3957529807	NC_000005.10:122071195:TGTG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss326757518, ss326981298, ss551538821, ss551705631	NC_000005.8:121434787:TG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss82980569, ss295242612	NC_000005.8:121434812:GT:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
28623267, ss663555351, ss666326496, ss1374416305, ss3732762191, ss5173845081, ss5835555004	NC_000005.9:121406888:TG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3838211142	NC_000005.9:121406890:TG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3064173200, ss4128173381, ss5265611885, ss5463604308, ss5710836372	NC_000005.10:122071193:TG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3807156673	NC_000005.10:122071195:TG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715575601, ss3957529808	NC_000005.10:122071197:TG:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3648156640	NC_000005.10:122071218:GT:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss42611398	NT_034772.6:29720785:GT:	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3829473591, ss5173845083	NC_000005.9:121406888::TG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4128173375, ss5265611887, ss5463604307, ss5710836374	NC_000005.10:122071193::TG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715575602, ss3957529809	NC_000005.10:122071199::TG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5173845084	NC_000005.9:121406888::TGTG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1374416306	NC_000005.9:121406890::TGTG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4128173376, ss5265611889, ss5463604309, ss5710836375	NC_000005.10:122071193::TGTG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715575603, ss3957529811	NC_000005.10:122071199::TGTG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4128173377, ss5265611888, ss5463604310	NC_000005.10:122071193::TGTGTG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4128173378	NC_000005.10:122071193::TGTGTGTG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4128173379	NC_000005.10:122071193::TGTGTGTGTG	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11080035094	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:122071193:TGTGTGTGTGT… NC_000005.10:122071193:TGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(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 rs35544795

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35544795