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rs121908486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908486(C;T)
Make rs121908486(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position32859932
GeneSLC7A9
is asnp
is mentioned by
dbSNPrs121908486
ebirs121908486
HLIrs121908486
Exacrs121908486
Varsomers121908486
Maprs121908486
PheGenIrs121908486
hapmaprs121908486
1000 genomesrs121908486
hgdprs121908486
ensemblrs121908486
gopubmedrs121908486
geneviewrs121908486
scholarrs121908486
googlers121908486
pharmgkbrs121908486
gwascentralrs121908486
openSNPrs121908486
23andMers121908486
23andMe allrs121908486
SNP Nexus

SNPshotrs121908486
SNPdbers121908486
MSV3drs121908486
GWAS Ctlgrs121908486
Max Magnitude0
OMIM604144
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908486(T;T)
Alt rs121908486(T;T)
Reference rs121908486(C;C)
Significance Pathogenic
Disease Cystinuria
Variation info
Gene SLC7A9
CLNDBN Cystinuria
Reversed 1
HGVS NC_000019.9:g.33350838G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006145.2,