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rs1057524572

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524572(C;G)
Make rs1057524572(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position34647538
GeneGALT
is asnp
is mentioned by
dbSNPrs1057524572
dbSNP (old)rs1057524572
ClinGenrs1057524572
ebirs1057524572
HLIrs1057524572
Exacrs1057524572
Gnomadrs1057524572
Varsomers1057524572
Maprs1057524572
PheGenIrs1057524572
Biobankrs1057524572
1000 genomesrs1057524572
hgdprs1057524572
ensemblrs1057524572
gopubmedrs1057524572
geneviewrs1057524572
scholarrs1057524572
googlers1057524572
pharmgkbrs1057524572
gwascentralrs1057524572
openSNPrs1057524572
23andMers1057524572
23andMe allrs1057524572
SNPshotrs1057524572
SNPdbers1057524572
MSV3drs1057524572
GWAS Ctlgrs1057524572
Max Magnitude0
ClinVar
Risk rs1057524572(G;G)
Alt rs1057524572(G;G)
Reference Rs1057524572(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GALT
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.34647535C>G
CLNSRC
CLNACC RCV000422602.1,