Name: rs5891669
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.

rs5891669

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:58136004-58136029 (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)₁₅ / del(T)₁₄ / del(T)₁₀ / d…
del(T)₁₅ / del(T)₁₄ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: (T)₂₆=0.3802 (1904/5008, 1000G)
delTTT=0.2438 (1113/4566, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM110B : 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	4566	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.5795	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTTTT=0.2438, TTTTTTTTTTTTTTTTTTTTTTTT=0.1743, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.684368	0.181384	0.134248	32
European	Sub	4538	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.5778	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTTTT=0.2446, TTTTTTTTTTTTTTTTTTTTTTTT=0.1752, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.683103	0.182201	0.134696	32
African	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	8	TTTTTTTTTTTTTTTTTTTTTTTTTT=0.5	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.4, TTTTTTTTTTTTTTTTTTTTTTTT=0.1, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	0.333333	0.333333	0.333333	0

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(T)₂₆=0.3802	delTTT=0.6198
1000Genomes	African	Sub	1322	(T)₂₆=0.4569	delTTT=0.5431
1000Genomes	East Asian	Sub	1008	(T)₂₆=0.3760	delTTT=0.6240
1000Genomes	Europe	Sub	1006	(T)₂₆=0.4235	delTTT=0.5765
1000Genomes	South Asian	Sub	978	(T)₂₆=0.276	delTTT=0.724
1000Genomes	American	Sub	694	(T)₂₆=0.324	delTTT=0.676
Allele Frequency Aggregator	Total	Global	4566	(T)₂₆=0.5795	del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0009, delTTT=0.2438, delTT=0.1743, delT=0.0015, dupT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	4538	(T)₂₆=0.5778	del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0009, delTTT=0.2446, delTT=0.1752, delT=0.0015, dupT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	12	(T)₂₆=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Other	Sub	8	(T)₂₆=0.5	del(T)₁₅=0.0, del(T)₁₄=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.4, delTT=0.1, delT=0.0, dupT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	Latin American 2	Sub	4	(T)₂₆=1.0	del(T)₁₅=0.0, del(T)₁₄=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₂₆=1.0	del(T)₁₅=0.0, del(T)₁₄=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	Asian	Sub	2	(T)₂₆=1.0	del(T)₁₅=0.0, del(T)₁₄=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₂₆=0	del(T)₁₅=0, del(T)₁₄=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dup(T)₄=0

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 8	NC_000008.11:g.58136015_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136016_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136020_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136021_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136022_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136023_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136024_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136025_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136026_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136027_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136028_58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136029del
GRCh38.p14 chr 8	NC_000008.11:g.58136029dup
GRCh38.p14 chr 8	NC_000008.11:g.58136028_58136029dup
GRCh38.p14 chr 8	NC_000008.11:g.58136027_58136029dup
GRCh38.p14 chr 8	NC_000008.11:g.58136026_58136029dup
GRCh37.p13 chr 8	NC_000008.10:g.59048574_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048575_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048579_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048580_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048581_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048582_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048583_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048584_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048585_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048586_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048587_59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048588del
GRCh37.p13 chr 8	NC_000008.10:g.59048588dup
GRCh37.p13 chr 8	NC_000008.10:g.59048587_59048588dup
GRCh37.p13 chr 8	NC_000008.10:g.59048586_59048588dup
GRCh37.p13 chr 8	NC_000008.10:g.59048585_59048588dup

Gene: FAM110B, family with sequence similarity 110 member B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FAM110B transcript variant 1	NM_001377989.1:c.-324-989… NM_001377989.1:c.-324-9892_-324-9878del	N/A	Intron Variant
FAM110B transcript variant 3	NM_001377997.1:c.-324-989… NM_001377997.1:c.-324-9892_-324-9878del	N/A	Intron Variant
FAM110B transcript variant 4	NM_001377998.1:c.-324-989… NM_001377998.1:c.-324-9892_-324-9878del	N/A	Intron Variant
FAM110B transcript variant 2	NM_147189.4:c.-324-9892_-… NM_147189.4:c.-324-9892_-324-9878del	N/A	Intron Variant
FAM110B transcript variant X1	XM_017013948.2:c.-324-989… XM_017013948.2:c.-324-9892_-324-9878del	N/A	Intron Variant
FAM110B transcript variant X2	XM_047422400.1:c.-324-989… XM_047422400.1:c.-324-9892_-324-9878del	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)₂₆=	del(T)₁₅	del(T)₁₄	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 8	NC_000008.11:g.58136004_58136029=	NC_000008.11:g.58136015_58136029del	NC_000008.11:g.58136016_58136029del	NC_000008.11:g.58136020_58136029del	NC_000008.11:g.58136021_58136029del	NC_000008.11:g.58136022_58136029del	NC_000008.11:g.58136023_58136029del	NC_000008.11:g.58136024_58136029del	NC_000008.11:g.58136025_58136029del	NC_000008.11:g.58136026_58136029del	NC_000008.11:g.58136027_58136029del	NC_000008.11:g.58136028_58136029del	NC_000008.11:g.58136029del	NC_000008.11:g.58136029dup	NC_000008.11:g.58136028_58136029dup	NC_000008.11:g.58136027_58136029dup	NC_000008.11:g.58136026_58136029dup
GRCh37.p13 chr 8	NC_000008.10:g.59048563_59048588=	NC_000008.10:g.59048574_59048588del	NC_000008.10:g.59048575_59048588del	NC_000008.10:g.59048579_59048588del	NC_000008.10:g.59048580_59048588del	NC_000008.10:g.59048581_59048588del	NC_000008.10:g.59048582_59048588del	NC_000008.10:g.59048583_59048588del	NC_000008.10:g.59048584_59048588del	NC_000008.10:g.59048585_59048588del	NC_000008.10:g.59048586_59048588del	NC_000008.10:g.59048587_59048588del	NC_000008.10:g.59048588del	NC_000008.10:g.59048588dup	NC_000008.10:g.59048587_59048588dup	NC_000008.10:g.59048586_59048588dup	NC_000008.10:g.59048585_59048588dup
FAM110B transcript variant 1	NM_001377989.1:c.-324-9903=	NM_001377989.1:c.-324-9892_-324-9878del	NM_001377989.1:c.-324-9891_-324-9878del	NM_001377989.1:c.-324-9887_-324-9878del	NM_001377989.1:c.-324-9886_-324-9878del	NM_001377989.1:c.-324-9885_-324-9878del	NM_001377989.1:c.-324-9884_-324-9878del	NM_001377989.1:c.-324-9883_-324-9878del	NM_001377989.1:c.-324-9882_-324-9878del	NM_001377989.1:c.-324-9881_-324-9878del	NM_001377989.1:c.-324-9880_-324-9878del	NM_001377989.1:c.-324-9879_-324-9878del	NM_001377989.1:c.-324-9878del	NM_001377989.1:c.-324-9878dup	NM_001377989.1:c.-324-9879_-324-9878dup	NM_001377989.1:c.-324-9880_-324-9878dup	NM_001377989.1:c.-324-9881_-324-9878dup
FAM110B transcript variant 3	NM_001377997.1:c.-324-9903=	NM_001377997.1:c.-324-9892_-324-9878del	NM_001377997.1:c.-324-9891_-324-9878del	NM_001377997.1:c.-324-9887_-324-9878del	NM_001377997.1:c.-324-9886_-324-9878del	NM_001377997.1:c.-324-9885_-324-9878del	NM_001377997.1:c.-324-9884_-324-9878del	NM_001377997.1:c.-324-9883_-324-9878del	NM_001377997.1:c.-324-9882_-324-9878del	NM_001377997.1:c.-324-9881_-324-9878del	NM_001377997.1:c.-324-9880_-324-9878del	NM_001377997.1:c.-324-9879_-324-9878del	NM_001377997.1:c.-324-9878del	NM_001377997.1:c.-324-9878dup	NM_001377997.1:c.-324-9879_-324-9878dup	NM_001377997.1:c.-324-9880_-324-9878dup	NM_001377997.1:c.-324-9881_-324-9878dup
FAM110B transcript variant 4	NM_001377998.1:c.-324-9903=	NM_001377998.1:c.-324-9892_-324-9878del	NM_001377998.1:c.-324-9891_-324-9878del	NM_001377998.1:c.-324-9887_-324-9878del	NM_001377998.1:c.-324-9886_-324-9878del	NM_001377998.1:c.-324-9885_-324-9878del	NM_001377998.1:c.-324-9884_-324-9878del	NM_001377998.1:c.-324-9883_-324-9878del	NM_001377998.1:c.-324-9882_-324-9878del	NM_001377998.1:c.-324-9881_-324-9878del	NM_001377998.1:c.-324-9880_-324-9878del	NM_001377998.1:c.-324-9879_-324-9878del	NM_001377998.1:c.-324-9878del	NM_001377998.1:c.-324-9878dup	NM_001377998.1:c.-324-9879_-324-9878dup	NM_001377998.1:c.-324-9880_-324-9878dup	NM_001377998.1:c.-324-9881_-324-9878dup
FAM110B transcript	NM_147189.2:c.-324-9903=	NM_147189.2:c.-324-9892_-324-9878del	NM_147189.2:c.-324-9891_-324-9878del	NM_147189.2:c.-324-9887_-324-9878del	NM_147189.2:c.-324-9886_-324-9878del	NM_147189.2:c.-324-9885_-324-9878del	NM_147189.2:c.-324-9884_-324-9878del	NM_147189.2:c.-324-9883_-324-9878del	NM_147189.2:c.-324-9882_-324-9878del	NM_147189.2:c.-324-9881_-324-9878del	NM_147189.2:c.-324-9880_-324-9878del	NM_147189.2:c.-324-9879_-324-9878del	NM_147189.2:c.-324-9878del	NM_147189.2:c.-324-9878dup	NM_147189.2:c.-324-9879_-324-9878dup	NM_147189.2:c.-324-9880_-324-9878dup	NM_147189.2:c.-324-9881_-324-9878dup
FAM110B transcript variant 2	NM_147189.4:c.-324-9903=	NM_147189.4:c.-324-9892_-324-9878del	NM_147189.4:c.-324-9891_-324-9878del	NM_147189.4:c.-324-9887_-324-9878del	NM_147189.4:c.-324-9886_-324-9878del	NM_147189.4:c.-324-9885_-324-9878del	NM_147189.4:c.-324-9884_-324-9878del	NM_147189.4:c.-324-9883_-324-9878del	NM_147189.4:c.-324-9882_-324-9878del	NM_147189.4:c.-324-9881_-324-9878del	NM_147189.4:c.-324-9880_-324-9878del	NM_147189.4:c.-324-9879_-324-9878del	NM_147189.4:c.-324-9878del	NM_147189.4:c.-324-9878dup	NM_147189.4:c.-324-9879_-324-9878dup	NM_147189.4:c.-324-9880_-324-9878dup	NM_147189.4:c.-324-9881_-324-9878dup
FAM110B transcript variant X1	XM_005251324.1:c.-324-9903=	XM_005251324.1:c.-324-9892_-324-9878del	XM_005251324.1:c.-324-9891_-324-9878del	XM_005251324.1:c.-324-9887_-324-9878del	XM_005251324.1:c.-324-9886_-324-9878del	XM_005251324.1:c.-324-9885_-324-9878del	XM_005251324.1:c.-324-9884_-324-9878del	XM_005251324.1:c.-324-9883_-324-9878del	XM_005251324.1:c.-324-9882_-324-9878del	XM_005251324.1:c.-324-9881_-324-9878del	XM_005251324.1:c.-324-9880_-324-9878del	XM_005251324.1:c.-324-9879_-324-9878del	XM_005251324.1:c.-324-9878del	XM_005251324.1:c.-324-9878dup	XM_005251324.1:c.-324-9879_-324-9878dup	XM_005251324.1:c.-324-9880_-324-9878dup	XM_005251324.1:c.-324-9881_-324-9878dup
FAM110B transcript variant X2	XM_005251325.1:c.-324-9903=	XM_005251325.1:c.-324-9892_-324-9878del	XM_005251325.1:c.-324-9891_-324-9878del	XM_005251325.1:c.-324-9887_-324-9878del	XM_005251325.1:c.-324-9886_-324-9878del	XM_005251325.1:c.-324-9885_-324-9878del	XM_005251325.1:c.-324-9884_-324-9878del	XM_005251325.1:c.-324-9883_-324-9878del	XM_005251325.1:c.-324-9882_-324-9878del	XM_005251325.1:c.-324-9881_-324-9878del	XM_005251325.1:c.-324-9880_-324-9878del	XM_005251325.1:c.-324-9879_-324-9878del	XM_005251325.1:c.-324-9878del	XM_005251325.1:c.-324-9878dup	XM_005251325.1:c.-324-9879_-324-9878dup	XM_005251325.1:c.-324-9880_-324-9878dup	XM_005251325.1:c.-324-9881_-324-9878dup
FAM110B transcript variant X3	XM_005251326.1:c.-324-9903=	XM_005251326.1:c.-324-9892_-324-9878del	XM_005251326.1:c.-324-9891_-324-9878del	XM_005251326.1:c.-324-9887_-324-9878del	XM_005251326.1:c.-324-9886_-324-9878del	XM_005251326.1:c.-324-9885_-324-9878del	XM_005251326.1:c.-324-9884_-324-9878del	XM_005251326.1:c.-324-9883_-324-9878del	XM_005251326.1:c.-324-9882_-324-9878del	XM_005251326.1:c.-324-9881_-324-9878del	XM_005251326.1:c.-324-9880_-324-9878del	XM_005251326.1:c.-324-9879_-324-9878del	XM_005251326.1:c.-324-9878del	XM_005251326.1:c.-324-9878dup	XM_005251326.1:c.-324-9879_-324-9878dup	XM_005251326.1:c.-324-9880_-324-9878dup	XM_005251326.1:c.-324-9881_-324-9878dup
FAM110B transcript variant X1	XM_017013948.2:c.-324-9903=	XM_017013948.2:c.-324-9892_-324-9878del	XM_017013948.2:c.-324-9891_-324-9878del	XM_017013948.2:c.-324-9887_-324-9878del	XM_017013948.2:c.-324-9886_-324-9878del	XM_017013948.2:c.-324-9885_-324-9878del	XM_017013948.2:c.-324-9884_-324-9878del	XM_017013948.2:c.-324-9883_-324-9878del	XM_017013948.2:c.-324-9882_-324-9878del	XM_017013948.2:c.-324-9881_-324-9878del	XM_017013948.2:c.-324-9880_-324-9878del	XM_017013948.2:c.-324-9879_-324-9878del	XM_017013948.2:c.-324-9878del	XM_017013948.2:c.-324-9878dup	XM_017013948.2:c.-324-9879_-324-9878dup	XM_017013948.2:c.-324-9880_-324-9878dup	XM_017013948.2:c.-324-9881_-324-9878dup
FAM110B transcript variant X2	XM_047422400.1:c.-324-9903=	XM_047422400.1:c.-324-9892_-324-9878del	XM_047422400.1:c.-324-9891_-324-9878del	XM_047422400.1:c.-324-9887_-324-9878del	XM_047422400.1:c.-324-9886_-324-9878del	XM_047422400.1:c.-324-9885_-324-9878del	XM_047422400.1:c.-324-9884_-324-9878del	XM_047422400.1:c.-324-9883_-324-9878del	XM_047422400.1:c.-324-9882_-324-9878del	XM_047422400.1:c.-324-9881_-324-9878del	XM_047422400.1:c.-324-9880_-324-9878del	XM_047422400.1:c.-324-9879_-324-9878del	XM_047422400.1:c.-324-9878del	XM_047422400.1:c.-324-9878dup	XM_047422400.1:c.-324-9879_-324-9878dup	XM_047422400.1:c.-324-9880_-324-9878dup	XM_047422400.1:c.-324-9881_-324-9878dup

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#.

56 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80955086	Aug 21, 2014 (142)
2	HGSV	ss81987291	Dec 15, 2007 (130)
3	HUMANGENOME_JCVI	ss95493055	Dec 05, 2013 (138)
4	PJP	ss295382491	Aug 21, 2014 (142)
5	PJP	ss295382492	May 09, 2011 (142)
6	1000GENOMES	ss1367946450	Aug 21, 2014 (142)
7	SWEGEN	ss3003241513	Nov 08, 2017 (151)
8	MCHAISSO	ss3066203735	Nov 08, 2017 (151)
9	URBANLAB	ss3648922710	Oct 12, 2018 (152)
10	EVA_DECODE	ss3722088718	Jul 13, 2019 (153)
11	EVA_DECODE	ss3722088719	Jul 13, 2019 (153)
12	EVA_DECODE	ss3722088720	Jul 13, 2019 (153)
13	EVA_DECODE	ss3722088721	Jul 13, 2019 (153)
14	EVA_DECODE	ss3722088722	Jul 13, 2019 (153)
15	ACPOP	ss3735694917	Jul 13, 2019 (153)
16	ACPOP	ss3735694918	Jul 13, 2019 (153)
17	PACBIO	ss3786155727	Jul 13, 2019 (153)
18	PACBIO	ss3791409903	Jul 13, 2019 (153)
19	PACBIO	ss3796291232	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3811203499	Jul 13, 2019 (153)
21	EVA	ss3831182345	Apr 26, 2020 (154)
22	GNOMAD	ss4185034585	Apr 26, 2021 (155)
23	GNOMAD	ss4185034586	Apr 26, 2021 (155)
24	GNOMAD	ss4185034587	Apr 26, 2021 (155)
25	GNOMAD	ss4185034589	Apr 26, 2021 (155)
26	GNOMAD	ss4185034590	Apr 26, 2021 (155)
27	GNOMAD	ss4185034591	Apr 26, 2021 (155)
28	GNOMAD	ss4185034592	Apr 26, 2021 (155)
29	GNOMAD	ss4185034593	Apr 26, 2021 (155)
30	GNOMAD	ss4185034594	Apr 26, 2021 (155)
31	GNOMAD	ss4185034595	Apr 26, 2021 (155)
32	GNOMAD	ss4185034596	Apr 26, 2021 (155)
33	GNOMAD	ss4185034597	Apr 26, 2021 (155)
34	GNOMAD	ss4185034598	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5188876089	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5188876090	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5188876091	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5188876092	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5188876093	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5277272850	Oct 17, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5277272851	Oct 17, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5277272852	Oct 17, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5277272853	Oct 17, 2022 (156)
44	HUGCELL_USP	ss5473826083	Oct 17, 2022 (156)
45	HUGCELL_USP	ss5473826084	Oct 17, 2022 (156)
46	HUGCELL_USP	ss5473826085	Oct 17, 2022 (156)
47	HUGCELL_USP	ss5473826086	Oct 17, 2022 (156)
48	TOMMO_GENOMICS	ss5730989704	Oct 17, 2022 (156)
49	TOMMO_GENOMICS	ss5730989705	Oct 17, 2022 (156)
50	TOMMO_GENOMICS	ss5730989706	Oct 17, 2022 (156)
51	TOMMO_GENOMICS	ss5730989707	Oct 17, 2022 (156)
52	TOMMO_GENOMICS	ss5730989708	Oct 17, 2022 (156)
53	EVA	ss5830584815	Oct 17, 2022 (156)
54	EVA	ss5830584816	Oct 17, 2022 (156)
55	EVA	ss5830584817	Oct 17, 2022 (156)
56	EVA	ss5830584818	Oct 17, 2022 (156)
57	1000Genomes	NC_000008.10 - 59048563	Oct 12, 2018 (152)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 297103781 (NC_000008.11:58136003::T 26/66726) Row 297103782 (NC_000008.11:58136003::TT 1/66724) Row 297103783 (NC_000008.11:58136003::TTT 2/66726)...	-	Apr 26, 2021 (155)
72	Northern Sweden Submission ignored due to conflicting rows: Row 8979782 (NC_000008.10:59048562:TTT: 7/600) Row 8979783 (NC_000008.10:59048562:TT: 2/600)	-	Jul 13, 2019 (153)
73	Northern Sweden Submission ignored due to conflicting rows: Row 8979782 (NC_000008.10:59048562:TTT: 7/600) Row 8979783 (NC_000008.10:59048562:TT: 2/600)	-	Jul 13, 2019 (153)
74	8.3KJPN Submission ignored due to conflicting rows: Row 46845396 (NC_000008.10:59048562:TTT: 5700/15970) Row 46845397 (NC_000008.10:59048562:TT: 1353/15970) Row 46845398 (NC_000008.10:59048562:T: 10/15970)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 46845396 (NC_000008.10:59048562:TTT: 5700/15970) Row 46845397 (NC_000008.10:59048562:TT: 1353/15970) Row 46845398 (NC_000008.10:59048562:T: 10/15970)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 46845396 (NC_000008.10:59048562:TTT: 5700/15970) Row 46845397 (NC_000008.10:59048562:TT: 1353/15970) Row 46845398 (NC_000008.10:59048562:T: 10/15970)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 46845396 (NC_000008.10:59048562:TTT: 5700/15970) Row 46845397 (NC_000008.10:59048562:TT: 1353/15970) Row 46845398 (NC_000008.10:59048562:T: 10/15970)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 46845396 (NC_000008.10:59048562:TTT: 5700/15970) Row 46845397 (NC_000008.10:59048562:TT: 1353/15970) Row 46845398 (NC_000008.10:59048562:T: 10/15970)...	-	Apr 26, 2021 (155)
79	14KJPN Submission ignored due to conflicting rows: Row 64826808 (NC_000008.11:58136003:TTT: 12674/27060) Row 64826809 (NC_000008.11:58136003:TT: 3094/27060) Row 64826810 (NC_000008.11:58136003:T: 18/27060)...	-	Oct 17, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 64826808 (NC_000008.11:58136003:TTT: 12674/27060) Row 64826809 (NC_000008.11:58136003:TT: 3094/27060) Row 64826810 (NC_000008.11:58136003:T: 18/27060)...	-	Oct 17, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 64826808 (NC_000008.11:58136003:TTT: 12674/27060) Row 64826809 (NC_000008.11:58136003:TT: 3094/27060) Row 64826810 (NC_000008.11:58136003:T: 18/27060)...	-	Oct 17, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 64826808 (NC_000008.11:58136003:TTT: 12674/27060) Row 64826809 (NC_000008.11:58136003:TT: 3094/27060) Row 64826810 (NC_000008.11:58136003:T: 18/27060)...	-	Oct 17, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 64826808 (NC_000008.11:58136003:TTT: 12674/27060) Row 64826809 (NC_000008.11:58136003:TT: 3094/27060) Row 64826810 (NC_000008.11:58136003:T: 18/27060)...	-	Oct 17, 2022 (156)
84	ALFA	NC_000008.11 - 58136004	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)
rs66474974	May 11, 2012 (137)
rs34721948	May 23, 2006 (127)
rs57029995	Oct 05, 2011 (135)
rs58279977	May 24, 2008 (130)
rs149977409	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4185034598, ss5277272853	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4185034597	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4185034596	NC_000008.11:58136003:TTTTTTTTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4185034595	NC_000008.11:58136003:TTTTTTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4185034594	NC_000008.11:58136003:TTTTTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4185034593	NC_000008.11:58136003:TTTTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5830584816	NC_000008.10:59048562:TTTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT
ss3722088718, ss4185034592	NC_000008.11:58136003:TTTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3003241513, ss3786155727, ss5188876092, ss5830584817	NC_000008.10:59048562:TTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185034591, ss5277272851, ss5473826085, ss5730989707	NC_000008.11:58136003:TTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3722088719	NC_000008.11:58136004:TTTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss295382491	NC_000008.9:59211116:TTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss81987291, ss295382492	NC_000008.9:59211139:TTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
42134614, ss1367946450, ss3735694917, ss3791409903, ss3796291232, ss5188876089, ss5830584815	NC_000008.10:59048562:TTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3648922710, ss3811203499, ss4185034590, ss5473826083, ss5730989704	NC_000008.11:58136003:TTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3722088720	NC_000008.11:58136005:TTT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss80955086	NC_000008.9:59211140:TT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3735694918, ss3831182345, ss5188876090, ss5830584818	NC_000008.10:59048562:TT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3066203735, ss4185034589, ss5473826084, ss5730989705	NC_000008.11:58136003:TT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3722088721	NC_000008.11:58136006:TT:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5188876091	NC_000008.10:59048562:T:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5277272850, ss5473826086, ss5730989706	NC_000008.11:58136003:T:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3722088722	NC_000008.11:58136007:T:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95493055	NT_008183.19:10912988:T:	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5188876093	NC_000008.10:59048562::T	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185034585, ss5277272852, ss5730989708	NC_000008.11:58136003::T	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185034586	NC_000008.11:58136003::TT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95493055	NT_008183.19:10912988:T:TTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4185034587	NC_000008.11:58136003::TTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2662679630	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:58136003:TTTTTTTTTTTT… NC_000008.11:58136003:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs5891669

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs5891669