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rs121918621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918621(A;A)
Make rs121918621(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31488919
GeneSLC5A2
is asnp
is mentioned by
dbSNPrs121918621
ebirs121918621
HLIrs121918621
Exacrs121918621
Varsomers121918621
Maprs121918621
PheGenIrs121918621
hapmaprs121918621
1000 genomesrs121918621
hgdprs121918621
ensemblrs121918621
gopubmedrs121918621
geneviewrs121918621
scholarrs121918621
googlers121918621
pharmgkbrs121918621
gwascentralrs121918621
openSNPrs121918621
23andMers121918621
23andMe allrs121918621
SNP Nexus

SNPshotrs121918621
SNPdbers121918621
MSV3drs121918621
GWAS Ctlgrs121918621
Max Magnitude0
OMIM182381
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918621(A;A)
Alt rs121918621(A;A)
Reference rs121918621(G;G)
Significance Pathogenic
Disease Familial renal glucosuria
Variation info
Gene SLC5A2
CLNDBN Familial renal glucosuria
Reversed 0
HGVS NC_000016.9:g.31500240G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013767.25,