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rs730881942

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881942(-;-)
Make rs730881942(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58692736
GeneRAD51C, TEX14
is asnp
is mentioned by
dbSNPrs730881942
ebirs730881942
HLIrs730881942
Exacrs730881942
Varsomers730881942
Maprs730881942
PheGenIrs730881942
hapmaprs730881942
1000 genomesrs730881942
hgdprs730881942
ensemblrs730881942
gopubmedrs730881942
geneviewrs730881942
scholarrs730881942
googlers730881942
pharmgkbrs730881942
gwascentralrs730881942
openSNPrs730881942
23andMers730881942
23andMe allrs730881942
SNP Nexus

SNPshotrs730881942
SNPdbers730881942
MSV3drs730881942
GWAS Ctlgrs730881942
Max Magnitude0
ClinVar
Risk rs730881942(;)
Alt rs730881942(;)
Reference rs730881942(G;G)
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.56770097delG
CLNSRC
CLNACC RCV000160936.3, RCV000205375.1, RCV000212931.1,