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rs730881939

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881939(-;-)
Make rs730881939(-;A)
Make rs730881939(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58695009
GeneRAD51C
is asnp
is mentioned by
dbSNPrs730881939
ebirs730881939
HLIrs730881939
Exacrs730881939
Varsomers730881939
Maprs730881939
PheGenIrs730881939
hapmaprs730881939
1000 genomesrs730881939
hgdprs730881939
ensemblrs730881939
gopubmedrs730881939
geneviewrs730881939
scholarrs730881939
googlers730881939
pharmgkbrs730881939
gwascentralrs730881939
openSNPrs730881939
23andMers730881939
23andMe allrs730881939
SNP Nexus

SNPshotrs730881939
SNPdbers730881939
MSV3drs730881939
GWAS Ctlgrs730881939
Max Magnitude0
ClinVar
Risk rs730881939(A;A)
Alt rs730881939(A;A)
Reference rs730881939(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Fanconi anemia
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O
Reversed 0
HGVS NC_000017.10:g.56772370dupA
CLNSRC
CLNACC RCV000160933.2, RCV000206050.1,