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rs587781995

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587781995(-;-)
Make rs587781995(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58724038
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs587781995
ebirs587781995
HLIrs587781995
Exacrs587781995
Varsomers587781995
Maprs587781995
PheGenIrs587781995
hapmaprs587781995
1000 genomesrs587781995
hgdprs587781995
ensemblrs587781995
gopubmedrs587781995
geneviewrs587781995
scholarrs587781995
googlers587781995
pharmgkbrs587781995
gwascentralrs587781995
openSNPrs587781995
23andMers587781995
23andMe allrs587781995
SNP Nexus

SNPshotrs587781995
SNPdbers587781995
MSV3drs587781995
GWAS Ctlgrs587781995
Max Magnitude0
ClinVar
Risk rs587781995(;)
Alt rs587781995(;)
Reference rs587781995(AG;AG)
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.56801399_56801400delAG
CLNSRC
CLNACC RCV000130408.2, RCV000236611.1,