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rs876660010

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660010(-;-)
Make rs876660010(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43051067
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660010
ebirs876660010
HLIrs876660010
Exacrs876660010
Varsomers876660010
Maprs876660010
PheGenIrs876660010
hapmaprs876660010
1000 genomesrs876660010
hgdprs876660010
ensemblrs876660010
gopubmedrs876660010
geneviewrs876660010
scholarrs876660010
googlers876660010
pharmgkbrs876660010
gwascentralrs876660010
openSNPrs876660010
23andMers876660010
23andMe allrs876660010
SNP Nexus

SNPshotrs876660010
SNPdbers876660010
MSV3drs876660010
GWAS Ctlgrs876660010
Max Magnitude0
ClinVar
Risk rs876660010(;)
Alt rs876660010(;)
Reference rs876660010(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.41203084delG
CLNSRC
CLNACC RCV000214451.1,