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rs796051968

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051968(A;A)
Make rs796051968(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position34649413
GeneGALT
is asnp
is mentioned by
dbSNPrs796051968
ebirs796051968
HLIrs796051968
Exacrs796051968
Varsomers796051968
Maprs796051968
PheGenIrs796051968
hapmaprs796051968
1000 genomesrs796051968
hgdprs796051968
ensemblrs796051968
gopubmedrs796051968
geneviewrs796051968
scholarrs796051968
googlers796051968
pharmgkbrs796051968
gwascentralrs796051968
openSNPrs796051968
23andMers796051968
23andMe allrs796051968
SNP Nexus

SNPshotrs796051968
SNPdbers796051968
MSV3drs796051968
GWAS Ctlgrs796051968
Max Magnitude0
ClinVar
Risk rs796051968(A;A)
Alt rs796051968(A;A)
Reference rs796051968(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GALT
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.34649410C>A
CLNSRC
CLNACC RCV000185921.1,