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rs273899689

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs273899689(CC;G)
Make rs273899689(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092718
GeneBRCA1
is asnp
is mentioned by
dbSNPrs273899689
ebirs273899689
HLIrs273899689
Exacrs273899689
Varsomers273899689
Maprs273899689
PheGenIrs273899689
hapmaprs273899689
1000 genomesrs273899689
hgdprs273899689
ensemblrs273899689
gopubmedrs273899689
geneviewrs273899689
scholarrs273899689
googlers273899689
pharmgkbrs273899689
gwascentralrs273899689
openSNPrs273899689
23andMers273899689
23andMe allrs273899689
SNP Nexus

SNPshotrs273899689
SNPdbers273899689
MSV3drs273899689
GWAS Ctlgrs273899689
Max Magnitude0
ClinVar
Risk rs273899689(G;G)
Alt rs273899689(G;G)
Reference rs273899689(CC;CC)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244735_41244736delGGinsC
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000047978.2, RCV000111943.1,