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rs770637624

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770637624(C;T)
Make rs770637624(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58709862
GeneRAD51C
is asnp
is mentioned by
dbSNPrs770637624
ebirs770637624
HLIrs770637624
Exacrs770637624
Varsomers770637624
Maprs770637624
PheGenIrs770637624
hapmaprs770637624
1000 genomesrs770637624
hgdprs770637624
ensemblrs770637624
gopubmedrs770637624
geneviewrs770637624
scholarrs770637624
googlers770637624
pharmgkbrs770637624
gwascentralrs770637624
openSNPrs770637624
23andMers770637624
23andMe allrs770637624
SNP Nexus

SNPshotrs770637624
SNPdbers770637624
MSV3drs770637624
GWAS Ctlgrs770637624
Max Magnitude0
ClinVar
Risk rs770637624(T;T)
Alt rs770637624(T;T)
Reference rs770637624(C;C)
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.56787223C>T
CLNSRC
CLNACC RCV000165947.1, RCV000233212.1,