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rs273897656

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs273897656(C;C)
Make rs273897656(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094212
GeneBRCA1
is asnp
is mentioned by
dbSNPrs273897656
ebirs273897656
HLIrs273897656
Exacrs273897656
Varsomers273897656
Maprs273897656
PheGenIrs273897656
hapmaprs273897656
1000 genomesrs273897656
hgdprs273897656
ensemblrs273897656
gopubmedrs273897656
geneviewrs273897656
scholarrs273897656
googlers273897656
pharmgkbrs273897656
gwascentralrs273897656
openSNPrs273897656
23andMers273897656
23andMe allrs273897656
SNP Nexus

SNPshotrs273897656
SNPdbers273897656
MSV3drs273897656
GWAS Ctlgrs273897656
Max Magnitude0
ClinVar
Risk rs273897656(C,G;C,G)
Alt rs273897656(C,G;C,G)
Reference rs273897656(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41246229A>C; NC_000017.10:g.41246229A>G
CLNSRC
CLNACC RCV000216490.1, RCV000047414.2, RCV000111587.1,