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rs121908484

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908484(C;T)
Make rs121908484(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position32843932
GeneSLC7A9
is asnp
is mentioned by
dbSNPrs121908484
ebirs121908484
HLIrs121908484
Exacrs121908484
Varsomers121908484
Maprs121908484
PheGenIrs121908484
hapmaprs121908484
1000 genomesrs121908484
hgdprs121908484
ensemblrs121908484
gopubmedrs121908484
geneviewrs121908484
scholarrs121908484
googlers121908484
pharmgkbrs121908484
gwascentralrs121908484
openSNPrs121908484
23andMers121908484
23andMe allrs121908484
SNP Nexus

SNPshotrs121908484
SNPdbers121908484
MSV3drs121908484
GWAS Ctlgrs121908484
Max Magnitude0
OMIM604144
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908484(T;T)
Alt rs121908484(T;T)
Reference rs121908484(C;C)
Significance Pathogenic
Disease Cystinuria
Variation info
Gene SLC7A9
CLNDBN Cystinuria
Reversed 1
HGVS NC_000019.9:g.33334838G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006143.2,