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rs1057517641

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517641(G;G)
Make rs1057517641(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position58692790
GeneRAD51C, TEX14
is asnp
is mentioned by
dbSNPrs1057517641
dbSNP (classic)rs1057517641
ClinGenrs1057517641
ebirs1057517641
HLIrs1057517641
Exacrs1057517641
Gnomadrs1057517641
Varsomers1057517641
LitVarrs1057517641
Maprs1057517641
PheGenIrs1057517641
Biobankrs1057517641
1000 genomesrs1057517641
hgdprs1057517641
ensemblrs1057517641
geneviewrs1057517641
scholarrs1057517641
googlers1057517641
pharmgkbrs1057517641
gwascentralrs1057517641
openSNPrs1057517641
23andMers1057517641
SNPshotrs1057517641
SNPdbers1057517641
MSV3drs1057517641
GWAS Ctlgrs1057517641
Max Magnitude0
ClinVar
Risk rs1057517641(G;G)
Alt rs1057517641(G;G)
Reference Rs1057517641(T;T)
Significance Probable-Pathogenic
Disease Fanconi anemia Breast-ovarian cancer
Variation info
Gene TEX14 RAD51C
CLNDBN Fanconi anemia, complementation group O Breast-ovarian cancer, familial 3
Reversed 0
HGVS NC_000017.10:g.56770151T>G
CLNSRC
CLNACC RCV000410256.1, RCV000411364.1,