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rs273899695

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs273899695(-;-)
Make rs273899695(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104263
GeneBRCA1
is asnp
is mentioned by
dbSNPrs273899695
ebirs273899695
HLIrs273899695
Exacrs273899695
Varsomers273899695
Maprs273899695
PheGenIrs273899695
hapmaprs273899695
1000 genomesrs273899695
hgdprs273899695
ensemblrs273899695
gopubmedrs273899695
geneviewrs273899695
scholarrs273899695
googlers273899695
pharmgkbrs273899695
gwascentralrs273899695
openSNPrs273899695
23andMers273899695
23andMe allrs273899695
SNP Nexus

SNPshotrs273899695
SNPdbers273899695
MSV3drs273899695
GWAS Ctlgrs273899695
Max Magnitude0
ClinVar
Risk rs273899695(;)
Alt rs273899695(;)
Reference rs273899695(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41256280delT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048047.5, RCV000077534.5, RCV000130037.2,