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rs876658644

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658644(A;A)
Make rs876658644(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58703330
GeneRAD51C
is asnp
is mentioned by
dbSNPrs876658644
ebirs876658644
HLIrs876658644
Exacrs876658644
Varsomers876658644
Maprs876658644
PheGenIrs876658644
hapmaprs876658644
1000 genomesrs876658644
hgdprs876658644
ensemblrs876658644
gopubmedrs876658644
geneviewrs876658644
scholarrs876658644
googlers876658644
pharmgkbrs876658644
gwascentralrs876658644
openSNPrs876658644
23andMers876658644
23andMe allrs876658644
SNP Nexus

SNPshotrs876658644
SNPdbers876658644
MSV3drs876658644
GWAS Ctlgrs876658644
Max Magnitude0
ClinVar
Risk rs876658644(A;A)
Alt rs876658644(A;A)
Reference rs876658644(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD51C
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.56780691G>A
CLNSRC
CLNACC RCV000218961.1,