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rs876660623

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660623(-;-)
Make rs876660623(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094279
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660623
ebirs876660623
HLIrs876660623
Exacrs876660623
Varsomers876660623
Maprs876660623
PheGenIrs876660623
hapmaprs876660623
1000 genomesrs876660623
hgdprs876660623
ensemblrs876660623
gopubmedrs876660623
geneviewrs876660623
scholarrs876660623
googlers876660623
pharmgkbrs876660623
gwascentralrs876660623
openSNPrs876660623
23andMers876660623
23andMe allrs876660623
SNP Nexus

SNPshotrs876660623
SNPdbers876660623
MSV3drs876660623
GWAS Ctlgrs876660623
Max Magnitude0
ClinVar
Risk rs876660623(;)
Alt rs876660623(;)
Reference rs876660623(G;G)
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.41246296delC
CLNSRC
CLNACC RCV000218101.1,