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dbSNP Short Genetic Variations

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.

rs772270559

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr9:14746379 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.000008 (2/264690, TOPMED)
G=0.000008 (2/248978, GnomAD_exome)
G=0.000000 (0/140282, GnomAD) (+ 2 more)
G=0.000017 (2/120640, ExAC)
G=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
FREM1 : Synonymous 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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 14050 A=1.00000 G=0.00000
European Sub 9690 A=1.0000 G=0.0000
African Sub 2898 A=1.0000 G=0.0000
African Others Sub 114 A=1.000 G=0.000
African American Sub 2784 A=1.0000 G=0.0000
Asian Sub 112 A=1.000 G=0.000
East Asian Sub 86 A=1.00 G=0.00
Other Asian Sub 26 A=1.00 G=0.00
Latin American 1 Sub 146 A=1.000 G=0.000
Latin American 2 Sub 610 A=1.000 G=0.000
South Asian Sub 98 A=1.00 G=0.00
Other Sub 496 A=1.000 G=0.000


Help

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

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 A=0.999992 G=0.000008
gnomAD - Exomes Global Study-wide 248978 A=0.999992 G=0.000008
gnomAD - Exomes European Sub 134348 A=0.999985 G=0.000015
gnomAD - Exomes Asian Sub 48562 A=1.00000 G=0.00000
gnomAD - Exomes American Sub 34496 A=1.00000 G=0.00000
gnomAD - Exomes African Sub 15478 A=1.00000 G=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10056 A=1.00000 G=0.00000
gnomAD - Exomes Other Sub 6038 A=1.0000 G=0.0000
gnomAD - Genomes Global Study-wide 140282 A=1.000000 G=0.000000
gnomAD - Genomes European Sub 75950 A=1.00000 G=0.00000
gnomAD - Genomes African Sub 42058 A=1.00000 G=0.00000
gnomAD - Genomes American Sub 13662 A=1.00000 G=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=1.0000 G=0.0000
gnomAD - Genomes East Asian Sub 3134 A=1.0000 G=0.0000
gnomAD - Genomes Other Sub 2154 A=1.0000 G=0.0000
ExAC Global Study-wide 120640 A=0.999983 G=0.000017
ExAC Europe Sub 73300 A=0.99997 G=0.00003
ExAC Asian Sub 25110 A=1.00000 G=0.00000
ExAC American Sub 11528 A=1.00000 G=0.00000
ExAC African Sub 9802 A=1.0000 G=0.0000
ExAC Other Sub 900 A=1.000 G=0.000
Allele Frequency Aggregator Total Global 14050 A=1.00000 G=0.00000
Allele Frequency Aggregator European Sub 9690 A=1.0000 G=0.0000
Allele Frequency Aggregator African Sub 2898 A=1.0000 G=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 A=1.000 G=0.000
Allele Frequency Aggregator Other Sub 496 A=1.000 G=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 A=1.000 G=0.000
Allele Frequency Aggregator Asian Sub 112 A=1.000 G=0.000
Allele Frequency Aggregator South Asian Sub 98 A=1.00 G=0.00
Help

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 9 NC_000009.12:g.14746379A>G
GRCh37.p13 chr 9 NC_000009.11:g.14746377A>G
FREM1 RefSeqGene NG_017005.2:g.168858T>C
Gene: FREM1, FRAS1 related extracellular matrix 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
FREM1 transcript variant 3 NM_001370058.2:c.1596+544…

NM_001370058.2:c.1596+544T>C

N/A Intron Variant
FREM1 transcript variant 4 NM_001370060.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant 6 NM_001370063.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant 7 NM_001370065.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant 13 NM_001379081.2:c.6228T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform 1 precursor NP_001366010.1:p.Asn2076= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant 5 NM_001370061.2:c.1836T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform 2 NP_001356990.1:p.Asn612= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant 1 NM_144966.7:c.6228T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform 1 precursor NP_659403.4:p.Asn2076= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant 2 NM_001177704.3:c.1836T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform 2 NP_001171175.1:p.Asn612= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant 8 NR_163238.2:n.5618T>C N/A Non Coding Transcript Variant
FREM1 transcript variant 9 NR_163239.2:n.7036T>C N/A Non Coding Transcript Variant
FREM1 transcript variant 12 NR_163242.2:n.2050T>C N/A Non Coding Transcript Variant
FREM1 transcript variant 10 NR_163240.1:n. N/A Genic Downstream Transcript Variant
FREM1 transcript variant 11 NR_163241.1:n. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X11 XM_017014325.3:c.6165+544…

XM_017014325.3:c.6165+544T>C

N/A Intron Variant
FREM1 transcript variant X29 XM_047422859.1:c.1632+544…

XM_047422859.1:c.1632+544T>C

N/A Intron Variant
FREM1 transcript variant X14 XM_017014328.3:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X15 XM_017014329.3:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X23 XM_017014330.3:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X16 XM_047422849.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X17 XM_047422850.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X18 XM_047422851.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X19 XM_047422852.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X20 XM_047422853.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X21 XM_047422854.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X22 XM_047422855.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X24 XM_047422856.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X25 XM_047422857.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X26 XM_047422858.1:c. N/A Genic Downstream Transcript Variant
FREM1 transcript variant X1 XM_017014316.3:c.6255T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869805.1:p.Asn2085= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X2 XM_047422844.1:c.6255T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X1 XP_047278800.1:p.Asn2085= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X30 XM_047422845.1:c.6255T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X1 XP_047278801.1:p.Asn2085= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X3 XM_017014319.3:c.6255T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869808.1:p.Asn2085= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X4 XM_017014320.3:c.6255T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869809.1:p.Asn2085= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X5 XM_017014321.3:c.6255T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869810.1:p.Asn2085= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X6 XM_017014322.2:c.6255T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869811.1:p.Asn2085= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X7 XM_047422846.1:c.6228T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X2 XP_047278802.1:p.Asn2076= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X8 XM_047422847.1:c.6228T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X2 XP_047278803.1:p.Asn2076= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X9 XM_047422848.1:c.6228T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X2 XP_047278804.1:p.Asn2076= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X10 XM_017014324.3:c.6105T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X3 XP_016869813.1:p.Asn2035= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X12 XM_017014326.2:c.5847T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X5 XP_016869815.1:p.Asn1949= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X13 XM_017014327.3:c.5331T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X6 XP_016869816.1:p.Asn1777= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X27 XM_011517758.3:c.1872T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X18 XP_011516060.1:p.Asn624= N (Asn) > N (Asn) Synonymous Variant
FREM1 transcript variant X28 XM_006716729.4:c.1836T>C N [AAT] > N [AAC] Coding Sequence Variant
FRAS1-related extracellular matrix protein 1 isoform X19 XP_006716792.1:p.Asn612= N (Asn) > N (Asn) Synonymous Variant
Help

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
Help

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

Placement A= G
GRCh38.p14 chr 9 NC_000009.12:g.14746379= NC_000009.12:g.14746379A>G
GRCh37.p13 chr 9 NC_000009.11:g.14746377= NC_000009.11:g.14746377A>G
FREM1 RefSeqGene NG_017005.2:g.168858= NG_017005.2:g.168858T>C
FREM1 transcript variant 1 NM_144966.7:c.6228= NM_144966.7:c.6228T>C
FREM1 transcript variant 1 NM_144966.6:c.6228= NM_144966.6:c.6228T>C
FREM1 transcript variant 1 NM_144966.5:c.6228= NM_144966.5:c.6228T>C
FREM1 transcript variant 2 NM_001177704.3:c.1836= NM_001177704.3:c.1836T>C
FREM1 transcript variant 2 NM_001177704.2:c.1836= NM_001177704.2:c.1836T>C
FREM1 transcript variant 2 NM_001177704.1:c.1836= NM_001177704.1:c.1836T>C
FREM1 transcript variant 9 NR_163239.2:n.7036= NR_163239.2:n.7036T>C
FREM1 transcript variant 9 NR_163239.1:n.7036= NR_163239.1:n.7036T>C
FREM1 transcript variant 13 NM_001379081.2:c.6228= NM_001379081.2:c.6228T>C
FREM1 transcript variant 13 NM_001379081.1:c.6228= NM_001379081.1:c.6228T>C
FREM1 transcript variant 8 NR_163238.2:n.5618= NR_163238.2:n.5618T>C
FREM1 transcript variant 8 NR_163238.1:n.5618= NR_163238.1:n.5618T>C
FREM1 transcript variant 5 NM_001370061.2:c.1836= NM_001370061.2:c.1836T>C
FREM1 transcript variant 5 NM_001370061.1:c.1836= NM_001370061.1:c.1836T>C
FREM1 transcript variant 12 NR_163242.2:n.2050= NR_163242.2:n.2050T>C
FREM1 transcript variant 12 NR_163242.1:n.2050= NR_163242.1:n.2050T>C
FREM1 transcript variant X28 XM_006716729.4:c.1836= XM_006716729.4:c.1836T>C
FREM1 transcript variant X21 XM_006716729.3:c.1836= XM_006716729.3:c.1836T>C
FREM1 transcript variant X18 XM_006716729.2:c.1836= XM_006716729.2:c.1836T>C
FREM1 transcript variant X10 XM_006716729.1:c.1836= XM_006716729.1:c.1836T>C
FREM1 transcript variant X3 XM_017014319.3:c.6255= XM_017014319.3:c.6255T>C
FREM1 transcript variant X3 XM_017014319.2:c.6255= XM_017014319.2:c.6255T>C
FREM1 transcript variant X4 XM_017014319.1:c.6255= XM_017014319.1:c.6255T>C
FREM1 transcript variant X4 XM_017014320.3:c.6255= XM_017014320.3:c.6255T>C
FREM1 transcript variant X4 XM_017014320.2:c.6255= XM_017014320.2:c.6255T>C
FREM1 transcript variant X5 XM_017014320.1:c.6255= XM_017014320.1:c.6255T>C
FREM1 transcript variant X1 XM_017014316.3:c.6255= XM_017014316.3:c.6255T>C
FREM1 transcript variant X1 XM_017014316.2:c.6255= XM_017014316.2:c.6255T>C
FREM1 transcript variant X1 XM_017014316.1:c.6255= XM_017014316.1:c.6255T>C
FREM1 transcript variant X10 XM_017014324.3:c.6105= XM_017014324.3:c.6105T>C
FREM1 transcript variant X9 XM_017014324.2:c.6105= XM_017014324.2:c.6105T>C
FREM1 transcript variant X10 XM_017014324.1:c.6105= XM_017014324.1:c.6105T>C
FREM1 transcript variant X5 XM_017014321.3:c.6255= XM_017014321.3:c.6255T>C
FREM1 transcript variant X5 XM_017014321.2:c.6255= XM_017014321.2:c.6255T>C
FREM1 transcript variant X6 XM_017014321.1:c.6255= XM_017014321.1:c.6255T>C
FREM1 transcript variant X13 XM_017014327.3:c.5331= XM_017014327.3:c.5331T>C
FREM1 transcript variant X12 XM_017014327.2:c.5331= XM_017014327.2:c.5331T>C
FREM1 transcript variant X13 XM_017014327.1:c.5331= XM_017014327.1:c.5331T>C
FREM1 transcript variant X27 XM_011517758.3:c.1872= XM_011517758.3:c.1872T>C
FREM1 transcript variant X20 XM_011517758.2:c.1872= XM_011517758.2:c.1872T>C
FREM1 transcript variant X16 XM_011517758.1:c.1872= XM_011517758.1:c.1872T>C
FREM1 transcript variant X6 XM_017014322.2:c.6255= XM_017014322.2:c.6255T>C
FREM1 transcript variant X6 XM_017014322.1:c.6255= XM_017014322.1:c.6255T>C
FREM1 transcript variant X12 XM_017014326.2:c.5847= XM_017014326.2:c.5847T>C
FREM1 transcript variant X11 XM_017014326.1:c.5847= XM_017014326.1:c.5847T>C
FREM1 transcript variant X30 XM_047422845.1:c.6255= XM_047422845.1:c.6255T>C
FREM1 transcript variant X9 XM_047422848.1:c.6228= XM_047422848.1:c.6228T>C
FREM1 transcript variant X2 XM_047422844.1:c.6255= XM_047422844.1:c.6255T>C
FREM1 transcript variant X7 XM_047422846.1:c.6228= XM_047422846.1:c.6228T>C
FREM1 transcript variant X8 XM_047422847.1:c.6228= XM_047422847.1:c.6228T>C
FRAS1-related extracellular matrix protein 1 isoform 1 precursor NP_659403.4:p.Asn2076= NP_659403.4:p.Asn2076=
FRAS1-related extracellular matrix protein 1 isoform 2 NP_001171175.1:p.Asn612= NP_001171175.1:p.Asn612=
FRAS1-related extracellular matrix protein 1 isoform 1 precursor NP_001366010.1:p.Asn2076= NP_001366010.1:p.Asn2076=
FRAS1-related extracellular matrix protein 1 isoform 2 NP_001356990.1:p.Asn612= NP_001356990.1:p.Asn612=
FRAS1-related extracellular matrix protein 1 isoform X19 XP_006716792.1:p.Asn612= XP_006716792.1:p.Asn612=
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869808.1:p.Asn2085= XP_016869808.1:p.Asn2085=
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869809.1:p.Asn2085= XP_016869809.1:p.Asn2085=
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869805.1:p.Asn2085= XP_016869805.1:p.Asn2085=
FRAS1-related extracellular matrix protein 1 isoform X3 XP_016869813.1:p.Asn2035= XP_016869813.1:p.Asn2035=
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869810.1:p.Asn2085= XP_016869810.1:p.Asn2085=
FRAS1-related extracellular matrix protein 1 isoform X6 XP_016869816.1:p.Asn1777= XP_016869816.1:p.Asn1777=
FRAS1-related extracellular matrix protein 1 isoform X18 XP_011516060.1:p.Asn624= XP_011516060.1:p.Asn624=
FRAS1-related extracellular matrix protein 1 isoform X1 XP_016869811.1:p.Asn2085= XP_016869811.1:p.Asn2085=
FRAS1-related extracellular matrix protein 1 isoform X5 XP_016869815.1:p.Asn1949= XP_016869815.1:p.Asn1949=
FRAS1-related extracellular matrix protein 1 isoform X1 XP_047278801.1:p.Asn2085= XP_047278801.1:p.Asn2085=
FRAS1-related extracellular matrix protein 1 isoform X2 XP_047278804.1:p.Asn2076= XP_047278804.1:p.Asn2076=
FRAS1-related extracellular matrix protein 1 isoform X1 XP_047278800.1:p.Asn2085= XP_047278800.1:p.Asn2085=
FRAS1-related extracellular matrix protein 1 isoform X2 XP_047278802.1:p.Asn2076= XP_047278802.1:p.Asn2076=
FRAS1-related extracellular matrix protein 1 isoform X2 XP_047278803.1:p.Asn2076= XP_047278803.1:p.Asn2076=
FREM1 transcript variant 3 NM_001370058.2:c.1596+544= NM_001370058.2:c.1596+544T>C
FREM1 transcript variant X11 XM_017014325.3:c.6165+544= XM_017014325.3:c.6165+544T>C
FREM1 transcript variant X29 XM_047422859.1:c.1632+544= XM_047422859.1:c.1632+544T>C
Help

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#.

4 SubSNP, 5 Frequency submissions
No Submitter Submission ID Date (Build)
1 EVA_EXAC ss1689423226 Apr 01, 2015 (144)
2 GNOMAD ss2737509815 Nov 08, 2017 (151)
3 GNOMAD ss4198150614 Apr 26, 2021 (155)
4 TOPMED ss4813804641 Apr 26, 2021 (155)
5 ExAC NC_000009.11 - 14746377 Oct 12, 2018 (152)
6 gnomAD - Genomes NC_000009.12 - 14746379 Apr 26, 2021 (155)
7 gnomAD - Exomes NC_000009.11 - 14746377 Jul 13, 2019 (153)
8 TopMed NC_000009.12 - 14746379 Apr 26, 2021 (155)
9 ALFA NC_000009.12 - 14746379 Apr 26, 2021 (155)
Help

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

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
9541078, 6688938, ss1689423226, ss2737509815 NC_000009.11:14746376:A:G NC_000009.12:14746378:A:G (self)
319104437, 651182202, 1964741210, ss4198150614, ss4813804641 NC_000009.12:14746378:A:G NC_000009.12:14746378:A:G (self)
Help

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

No publications for rs772270559

Help

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.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07