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rs121908856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908856(A;C)
Make rs121908856(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position71447706
GeneSLC4A4
is asnp
is mentioned by
dbSNPrs121908856
ebirs121908856
HLIrs121908856
Exacrs121908856
Varsomers121908856
Maprs121908856
PheGenIrs121908856
hapmaprs121908856
1000 genomesrs121908856
hgdprs121908856
ensemblrs121908856
gopubmedrs121908856
geneviewrs121908856
scholarrs121908856
googlers121908856
pharmgkbrs121908856
gwascentralrs121908856
openSNPrs121908856
23andMers121908856
23andMe allrs121908856
SNP Nexus

SNPshotrs121908856
SNPdbers121908856
MSV3drs121908856
GWAS Ctlgrs121908856
Max Magnitude0
OMIM603345
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908856(C;C)
Alt rs121908856(C;C)
Reference rs121908856(A;A)
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.72313423A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006844.2,