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rs587782848

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782848(A;A)
Make rs587782848(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35107376
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs587782848
ebirs587782848
HLIrs587782848
Exacrs587782848
Varsomers587782848
Maprs587782848
PheGenIrs587782848
hapmaprs587782848
1000 genomesrs587782848
hgdprs587782848
ensemblrs587782848
gopubmedrs587782848
geneviewrs587782848
scholarrs587782848
googlers587782848
pharmgkbrs587782848
gwascentralrs587782848
openSNPrs587782848
23andMers587782848
23andMe allrs587782848
SNP Nexus

SNPshotrs587782848
SNPdbers587782848
MSV3drs587782848
GWAS Ctlgrs587782848
Max Magnitude0
ClinVar
Risk rs587782848(A,C;A,C)
Alt rs587782848(A,C;A,C)
Reference rs587782848(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.33434395C>G; NC_000017.10:g.33434395C>T
CLNSRC
CLNACC RCV000223012.1, RCV000132446.2,