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rs587780835

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587780835(A;G)
Make rs587780835(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58734116
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs587780835
ebirs587780835
HLIrs587780835
Exacrs587780835
Varsomers587780835
Maprs587780835
PheGenIrs587780835
hapmaprs587780835
1000 genomesrs587780835
hgdprs587780835
ensemblrs587780835
gopubmedrs587780835
geneviewrs587780835
scholarrs587780835
googlers587780835
pharmgkbrs587780835
gwascentralrs587780835
openSNPrs587780835
23andMers587780835
23andMe allrs587780835
SNP Nexus

SNPshotrs587780835
SNPdbers587780835
MSV3drs587780835
GWAS Ctlgrs587780835
Max Magnitude0
ClinVar
Risk rs587780835(G;G)
Alt rs587780835(G;G)
Reference rs587780835(A;A)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene RAD51C
CLNDBN Fanconi anemia, complementation group O
Reversed 0
HGVS NC_000017.10:g.56811477A>G
CLNSRC
CLNACC RCV000123368.1,