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rs587780840

From SNPedia

Orientationplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587780840(-;-)
Make rs587780840(-;CA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58692740
GeneRAD51C, TEX14
is asnp
is mentioned by
dbSNPrs587780840
ebirs587780840
HLIrs587780840
Exacrs587780840
Varsomers587780840
Maprs587780840
PheGenIrs587780840
hapmaprs587780840
1000 genomesrs587780840
hgdprs587780840
ensemblrs587780840
gopubmedrs587780840
geneviewrs587780840
scholarrs587780840
googlers587780840
pharmgkbrs587780840
gwascentralrs587780840
openSNPrs587780840
23andMers587780840
23andMe allrs587780840
SNP Nexus

SNPshotrs587780840
SNPdbers587780840
MSV3drs587780840
GWAS Ctlgrs587780840
Max Magnitude0
ClinVar
Risk rs587780840(;)
Alt rs587780840(;)
Reference rs587780840(CA;CA)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene TEX14 RAD51C
CLNDBN Fanconi anemia, complementation group O
Reversed 0
HGVS NC_000017.10:g.56770101_56770102delCA
CLNSRC
CLNACC RCV000123379.1,