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rs786205460

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205460(C;T)
Make rs786205460(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position89441152
GeneSLC16A12
is asnp
is mentioned by
dbSNPrs786205460
ebirs786205460
HLIrs786205460
Exacrs786205460
Varsomers786205460
Maprs786205460
PheGenIrs786205460
hapmaprs786205460
1000 genomesrs786205460
hgdprs786205460
ensemblrs786205460
gopubmedrs786205460
geneviewrs786205460
scholarrs786205460
googlers786205460
pharmgkbrs786205460
gwascentralrs786205460
openSNPrs786205460
23andMers786205460
23andMe allrs786205460
SNP Nexus

SNPshotrs786205460
SNPdbers786205460
MSV3drs786205460
GWAS Ctlgrs786205460
Max Magnitude0
ClinVar
Risk rs786205460(T;T)
Alt rs786205460(T;T)
Reference rs786205460(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC16A12
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.91200909G>A
CLNSRC
CLNACC RCV000171182.1,