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rs587781490

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781490(A;T)
Make rs587781490(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58696790
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587781490
ebirs587781490
HLIrs587781490
Exacrs587781490
Varsomers587781490
Maprs587781490
PheGenIrs587781490
hapmaprs587781490
1000 genomesrs587781490
hgdprs587781490
ensemblrs587781490
gopubmedrs587781490
geneviewrs587781490
scholarrs587781490
googlers587781490
pharmgkbrs587781490
gwascentralrs587781490
openSNPrs587781490
23andMers587781490
23andMe allrs587781490
SNP Nexus

SNPshotrs587781490
SNPdbers587781490
MSV3drs587781490
GWAS Ctlgrs587781490
Max Magnitude0
ClinVar
Risk rs587781490(G,T;G,T)
Alt rs587781490(G,T;G,T)
Reference rs587781490(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000017.10:g.56774151A>T
CLNSRC
CLNACC RCV000129454.4, RCV000212939.1,