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rs876659497

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs876659497(-;-)
Make rs876659497(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58703246
GeneRAD51C
is asnp
is mentioned by
dbSNPrs876659497
ebirs876659497
HLIrs876659497
Exacrs876659497
Varsomers876659497
Maprs876659497
PheGenIrs876659497
hapmaprs876659497
1000 genomesrs876659497
hgdprs876659497
ensemblrs876659497
gopubmedrs876659497
geneviewrs876659497
scholarrs876659497
googlers876659497
pharmgkbrs876659497
gwascentralrs876659497
openSNPrs876659497
23andMers876659497
23andMe allrs876659497
SNP Nexus

SNPshotrs876659497
SNPdbers876659497
MSV3drs876659497
GWAS Ctlgrs876659497
Max Magnitude0
ClinVar
Risk rs876659497(;)
Alt rs876659497(;)
Reference rs876659497(AT;AT)
Significance 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.56780607_56780608delAT
CLNSRC
CLNACC RCV000214716.1,