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rs758430398

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758430398(A;A)
Make rs758430398(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position34647206
GeneGALT
is asnp
is mentioned by
dbSNPrs758430398
ebirs758430398
HLIrs758430398
Exacrs758430398
Varsomers758430398
Maprs758430398
PheGenIrs758430398
hapmaprs758430398
1000 genomesrs758430398
hgdprs758430398
ensemblrs758430398
gopubmedrs758430398
geneviewrs758430398
scholarrs758430398
googlers758430398
pharmgkbrs758430398
gwascentralrs758430398
openSNPrs758430398
23andMers758430398
23andMe allrs758430398
SNP Nexus

SNPshotrs758430398
SNPdbers758430398
MSV3drs758430398
GWAS Ctlgrs758430398
Max Magnitude0
ClinVar
Risk rs758430398(A;A)
Alt rs758430398(A;A)
Reference rs758430398(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GALT
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.34647203G>A
CLNSRC
CLNACC RCV000185910.1,