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rs786203081

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs786203081(-;-)
Make rs786203081(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position58703277
GeneRAD51C
is asnp
is mentioned by
dbSNPrs786203081
ebirs786203081
HLIrs786203081
Exacrs786203081
Varsomers786203081
Maprs786203081
PheGenIrs786203081
hapmaprs786203081
1000 genomesrs786203081
hgdprs786203081
ensemblrs786203081
gopubmedrs786203081
geneviewrs786203081
scholarrs786203081
googlers786203081
pharmgkbrs786203081
gwascentralrs786203081
openSNPrs786203081
23andMers786203081
23andMe allrs786203081
SNP Nexus

SNPshotrs786203081
SNPdbers786203081
MSV3drs786203081
GWAS Ctlgrs786203081
Max Magnitude0
ClinVar
Risk rs786203081(;)
Alt rs786203081(;)
Reference rs786203081(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56780638_56780639delAG
CLNSRC
CLNACC RCV000166223.2,