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rs779582317

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs779582317(A;C)
Make rs779582317(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position58724038
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs779582317
ebirs779582317
HLIrs779582317
Exacrs779582317
Varsomers779582317
Maprs779582317
PheGenIrs779582317
hapmaprs779582317
1000 genomesrs779582317
hgdprs779582317
ensemblrs779582317
gopubmedrs779582317
geneviewrs779582317
scholarrs779582317
googlers779582317
pharmgkbrs779582317
gwascentralrs779582317
openSNPrs779582317
23andMers779582317
23andMe allrs779582317
SNP Nexus

SNPshotrs779582317
SNPdbers779582317
MSV3drs779582317
GWAS Ctlgrs779582317
Max Magnitude0
ClinVar
Risk rs779582317(C;C)
Alt rs779582317(C;C)
Reference rs779582317(A;A)
Significance Pathogenic
Disease Fanconi anemia not provided
Variation info
Gene RAD51C
CLNDBN Fanconi anemia, complementation group O not provided
Reversed 0
HGVS NC_000017.10:g.56801399A>C; NC_000017.10:g.56801399A>G
CLNSRC
CLNACC RCV000199789.1, RCV000236382.1,