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rs796051945

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051945(G;T)
Make rs796051945(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position100206250
GeneDBT
is asnp
is mentioned by
dbSNPrs796051945
ebirs796051945
HLIrs796051945
Exacrs796051945
Varsomers796051945
Maprs796051945
PheGenIrs796051945
hapmaprs796051945
1000 genomesrs796051945
hgdprs796051945
ensemblrs796051945
gopubmedrs796051945
geneviewrs796051945
scholarrs796051945
googlers796051945
pharmgkbrs796051945
gwascentralrs796051945
openSNPrs796051945
23andMers796051945
23andMe allrs796051945
SNP Nexus

SNPshotrs796051945
SNPdbers796051945
MSV3drs796051945
GWAS Ctlgrs796051945
Max Magnitude0
ClinVar
Risk rs796051945(T;T)
Alt rs796051945(T;T)
Reference rs796051945(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DBT
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.100671806C>A
CLNSRC
CLNACC RCV000185843.1,