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rs786201909

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786201909(G;G)
Make rs786201909(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position58703254
GeneRAD51C
is asnp
is mentioned by
dbSNPrs786201909
ebirs786201909
HLIrs786201909
Exacrs786201909
Varsomers786201909
Maprs786201909
PheGenIrs786201909
hapmaprs786201909
1000 genomesrs786201909
hgdprs786201909
ensemblrs786201909
gopubmedrs786201909
geneviewrs786201909
scholarrs786201909
googlers786201909
pharmgkbrs786201909
gwascentralrs786201909
openSNPrs786201909
23andMers786201909
23andMe allrs786201909
SNP Nexus

SNPshotrs786201909
SNPdbers786201909
MSV3drs786201909
GWAS Ctlgrs786201909
Max Magnitude0
ClinVar
Risk rs786201909(G;G)
Alt rs786201909(G;G)
Reference rs786201909(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56780615T>G
CLNSRC
CLNACC RCV000164432.1,