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rs1800461

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1800461(A;A)
Make rs1800461(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position34647190
GeneGALT
is asnp
is mentioned by
dbSNPrs1800461
ebirs1800461
HLIrs1800461
Exacrs1800461
Varsomers1800461
Maprs1800461
PheGenIrs1800461
hapmaprs1800461
1000 genomesrs1800461
hgdprs1800461
ensemblrs1800461
gopubmedrs1800461
geneviewrs1800461
scholarrs1800461
googlers1800461
pharmgkbrs1800461
gwascentralrs1800461
openSNPrs1800461
23andMers1800461
23andMe allrs1800461
SNP Nexus

SNPshotrs1800461
SNPdbers1800461
MSV3drs1800461
GWAS Ctlgrs1800461
Max Magnitude0
OMIM606999
Desc
Variant0004
Relatedalso
ClinVar
Risk rs1800461(A;A)
Alt rs1800461(A;A)
Reference rs1800461(C;C)
Significance Non-pathogenic
Disease GALT POLYMORPHISM Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Variation info
Gene GALT
CLNDBN GALT POLYMORPHISM Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Reversed 0
HGVS NC_000009.11:g.34647187C>A
CLNSRC ARUP GALT OMIM Allelic Variant
CLNACC RCV000003796.2, RCV000022064.1,