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rs730881931

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881931(C;C)
Make rs730881931(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58695191
GeneRAD51C
is asnp
is mentioned by
dbSNPrs730881931
dbSNP (old)rs730881931
ClinGenrs730881931
ebirs730881931
HLIrs730881931
Exacrs730881931
Varsomers730881931
Maprs730881931
PheGenIrs730881931
Biobankrs730881931
1000 genomesrs730881931
hgdprs730881931
ensemblrs730881931
gopubmedrs730881931
geneviewrs730881931
scholarrs730881931
googlers730881931
pharmgkbrs730881931
gwascentralrs730881931
openSNPrs730881931
23andMers730881931
23andMe allrs730881931
SNP Nexus

SNPshotrs730881931
SNPdbers730881931
MSV3drs730881931
GWAS Ctlgrs730881931
Max Magnitude0
ClinVar
Risk rs730881931(C;C)
Alt rs730881931(C;C)
Reference Rs730881931(T;T)
Significance Probable-Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome Fanconi anemia
Variation info
Gene RAD51C
CLNDBN not provided Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O
Reversed 0
HGVS NC_000017.10:g.56772552T>C
CLNSRC
CLNACC RCV000160923.2, RCV000221514.1, RCV000467500.1,