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rs876660194

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660194(-;-)
Make rs876660194(-;A)
Make rs876660194(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092241
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660194
ebirs876660194
HLIrs876660194
Exacrs876660194
Varsomers876660194
Maprs876660194
PheGenIrs876660194
hapmaprs876660194
1000 genomesrs876660194
hgdprs876660194
ensemblrs876660194
gopubmedrs876660194
geneviewrs876660194
scholarrs876660194
googlers876660194
pharmgkbrs876660194
gwascentralrs876660194
openSNPrs876660194
23andMers876660194
23andMe allrs876660194
SNP Nexus

SNPshotrs876660194
SNPdbers876660194
MSV3drs876660194
GWAS Ctlgrs876660194
Max Magnitude0
ClinVar
Risk rs876660194(A;A)
Alt rs876660194(A;A)
Reference rs876660194(;)
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.41244259dupT
CLNSRC
CLNACC RCV000221558.1,