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rs876660601

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660601(C;T)
Make rs876660601(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43090967
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660601
ebirs876660601
HLIrs876660601
Exacrs876660601
Varsomers876660601
Maprs876660601
PheGenIrs876660601
hapmaprs876660601
1000 genomesrs876660601
hgdprs876660601
ensemblrs876660601
gopubmedrs876660601
geneviewrs876660601
scholarrs876660601
googlers876660601
pharmgkbrs876660601
gwascentralrs876660601
openSNPrs876660601
23andMers876660601
23andMe allrs876660601
SNP Nexus

SNPshotrs876660601
SNPdbers876660601
MSV3drs876660601
GWAS Ctlgrs876660601
Max Magnitude0
ClinVar
Risk rs876660601(T;T)
Alt rs876660601(T;T)
Reference rs876660601(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41242984G>A
CLNSRC
CLNACC RCV000215519.1,