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rs121908858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908858(C;T)
Make rs121908858(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position71339333
GeneSLC4A4
is asnp
is mentioned by
dbSNPrs121908858
ebirs121908858
HLIrs121908858
Exacrs121908858
Varsomers121908858
Maprs121908858
PheGenIrs121908858
hapmaprs121908858
1000 genomesrs121908858
hgdprs121908858
ensemblrs121908858
gopubmedrs121908858
geneviewrs121908858
scholarrs121908858
googlers121908858
pharmgkbrs121908858
gwascentralrs121908858
openSNPrs121908858
23andMers121908858
23andMe allrs121908858
SNP Nexus

SNPshotrs121908858
SNPdbers121908858
MSV3drs121908858
GWAS Ctlgrs121908858
Max Magnitude0
OMIM603345
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908858(T;T)
Alt rs121908858(T;T)
Reference rs121908858(C;C)
Significance Pathogenic
Disease Renal tubular acidosis
Variation info
Gene SLC4A4
CLNDBN Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation
Reversed 0
HGVS NC_000004.11:g.72205050C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006846.2,