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rs267606997

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606997(A;A)
Make rs267606997(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position58709926
GeneRAD51C
is asnp
is mentioned by
dbSNPrs267606997
ebirs267606997
HLIrs267606997
Exacrs267606997
Varsomers267606997
Maprs267606997
PheGenIrs267606997
hapmaprs267606997
1000 genomesrs267606997
hgdprs267606997
ensemblrs267606997
gopubmedrs267606997
geneviewrs267606997
scholarrs267606997
googlers267606997
pharmgkbrs267606997
gwascentralrs267606997
openSNPrs267606997
23andMers267606997
23andMe allrs267606997
SNP Nexus

SNPshotrs267606997
SNPdbers267606997
MSV3drs267606997
GWAS Ctlgrs267606997
Max Magnitude0
ClinVar
Risk rs267606997(A;A)
Alt rs267606997(A;A)
Reference rs267606997(G;G)
Significance Pathogenic
Disease Fanconi anemia Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Fanconi anemia, complementation group O Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56787287G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007224.2, RCV000131703.2,