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rs398122801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122801(A;A)
Make rs398122801(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position31484657
GeneSLC5A2
is asnp
is mentioned by
dbSNPrs398122801
ebirs398122801
HLIrs398122801
Exacrs398122801
Varsomers398122801
Maprs398122801
PheGenIrs398122801
hapmaprs398122801
1000 genomesrs398122801
hgdprs398122801
ensemblrs398122801
gopubmedrs398122801
geneviewrs398122801
scholarrs398122801
googlers398122801
pharmgkbrs398122801
gwascentralrs398122801
openSNPrs398122801
23andMers398122801
23andMe allrs398122801
SNP Nexus

SNPshotrs398122801
SNPdbers398122801
MSV3drs398122801
GWAS Ctlgrs398122801
Max Magnitude0
ClinVar
Risk rs398122801(A,T;A,T)
Alt rs398122801(A,T;A,T)
Reference rs398122801(C;C)
Significance Pathogenic
Disease Familial renal glucosuria
Variation info
Gene SLC5A2
CLNDBN Familial renal glucosuria
Reversed 0
HGVS NC_000016.10:g.31484657C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022761.25,