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rs786202563

From SNPedia

Orientationplus
Geno Mag Summary
(AAACC;AAACC) 0 common in clinvar
Make rs786202563(-;-)
Make rs786202563(-;ACCAA)
Make rs786202563(ACCAA;ACCAA)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position58695001
GeneRAD51C
is asnp
is mentioned by
dbSNPrs786202563
ebirs786202563
HLIrs786202563
Exacrs786202563
Varsomers786202563
Maprs786202563
PheGenIrs786202563
hapmaprs786202563
1000 genomesrs786202563
hgdprs786202563
ensemblrs786202563
gopubmedrs786202563
geneviewrs786202563
scholarrs786202563
googlers786202563
pharmgkbrs786202563
gwascentralrs786202563
openSNPrs786202563
23andMers786202563
23andMe allrs786202563
SNP Nexus

SNPshotrs786202563
SNPdbers786202563
MSV3drs786202563
GWAS Ctlgrs786202563
Max Magnitude0
ClinVar
Risk rs786202563(;)
Alt rs786202563(;)
Reference rs786202563(AAACC;AAACC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56772362_56772366delACCAA
CLNSRC
CLNACC RCV000165425.1,