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rs587782528

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782528(C;T)
Make rs587782528(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58692740
GeneRAD51C, TEX14
is asnp
is mentioned by
dbSNPrs587782528
ebirs587782528
HLIrs587782528
Exacrs587782528
Varsomers587782528
Maprs587782528
PheGenIrs587782528
hapmaprs587782528
1000 genomesrs587782528
hgdprs587782528
ensemblrs587782528
gopubmedrs587782528
geneviewrs587782528
scholarrs587782528
googlers587782528
pharmgkbrs587782528
gwascentralrs587782528
openSNPrs587782528
23andMers587782528
23andMe allrs587782528
SNP Nexus

SNPshotrs587782528
SNPdbers587782528
MSV3drs587782528
GWAS Ctlgrs587782528
Max Magnitude0
ClinVar
Risk rs587782528(T;T)
Alt rs587782528(T;T)
Reference rs587782528(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Fanconi anemia not provided
Variation info
Gene TEX14 RAD51C
CLNDBN Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided
Reversed 0
HGVS NC_000017.10:g.56770101C>T
CLNSRC
CLNACC RCV000131716.4, RCV000196217.1, RCV000212932.1,