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rs1057523885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523885(A;A)
Make rs1057523885(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position34647657
GeneGALT
is asnp
is mentioned by
dbSNPrs1057523885
dbSNP (old)rs1057523885
ClinGenrs1057523885
ebirs1057523885
HLIrs1057523885
Exacrs1057523885
Gnomadrs1057523885
Varsomers1057523885
Maprs1057523885
PheGenIrs1057523885
Biobankrs1057523885
1000 genomesrs1057523885
hgdprs1057523885
ensemblrs1057523885
gopubmedrs1057523885
geneviewrs1057523885
scholarrs1057523885
googlers1057523885
pharmgkbrs1057523885
gwascentralrs1057523885
openSNPrs1057523885
23andMers1057523885
23andMe allrs1057523885
SNPshotrs1057523885
SNPdbers1057523885
MSV3drs1057523885
GWAS Ctlgrs1057523885
Max Magnitude0
ClinVar
Risk rs1057523885(A;A)
Alt rs1057523885(A;A)
Reference Rs1057523885(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GALT
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.34647654G>A
CLNSRC
CLNACC RCV000439035.1,