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rs587782699

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782699(-;-)
Make rs587782699(-;TA)
Make rs587782699(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58696790
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587782699
ebirs587782699
HLIrs587782699
Exacrs587782699
Varsomers587782699
Maprs587782699
PheGenIrs587782699
hapmaprs587782699
1000 genomesrs587782699
hgdprs587782699
ensemblrs587782699
gopubmedrs587782699
geneviewrs587782699
scholarrs587782699
googlers587782699
pharmgkbrs587782699
gwascentralrs587782699
openSNPrs587782699
23andMers587782699
23andMe allrs587782699
SNP Nexus

SNPshotrs587782699
SNPdbers587782699
MSV3drs587782699
GWAS Ctlgrs587782699
Max Magnitude0
ClinVar
Risk rs587782699(AT;AT)
Alt rs587782699(AT;AT)
Reference rs587782699(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56774150_56774151dupTA
CLNSRC
CLNACC RCV000132139.2,