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rs757128712

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757128712(A;A)
Make rs757128712(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58692789
GeneRAD51C, TEX14
is asnp
is mentioned by
dbSNPrs757128712
ebirs757128712
HLIrs757128712
Exacrs757128712
Varsomers757128712
Maprs757128712
PheGenIrs757128712
hapmaprs757128712
1000 genomesrs757128712
hgdprs757128712
ensemblrs757128712
gopubmedrs757128712
geneviewrs757128712
scholarrs757128712
googlers757128712
pharmgkbrs757128712
gwascentralrs757128712
openSNPrs757128712
23andMers757128712
23andMe allrs757128712
SNP Nexus

SNPshotrs757128712
SNPdbers757128712
MSV3drs757128712
GWAS Ctlgrs757128712
Max Magnitude0
ClinVar
Risk rs757128712(A;A)
Alt rs757128712(A;A)
Reference rs757128712(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TEX14 RAD51C
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.56770150G>T
CLNSRC
CLNACC RCV000216860.1,