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rs121908487

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908487(A;G)
Make rs121908487(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position32862127
GeneSLC7A9
is asnp
is mentioned by
dbSNPrs121908487
ebirs121908487
HLIrs121908487
Exacrs121908487
Varsomers121908487
Maprs121908487
PheGenIrs121908487
hapmaprs121908487
1000 genomesrs121908487
hgdprs121908487
ensemblrs121908487
gopubmedrs121908487
geneviewrs121908487
scholarrs121908487
googlers121908487
pharmgkbrs121908487
gwascentralrs121908487
openSNPrs121908487
23andMers121908487
23andMe allrs121908487
SNP Nexus

SNPshotrs121908487
SNPdbers121908487
MSV3drs121908487
GWAS Ctlgrs121908487
Max Magnitude0
OMIM604144
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121908487(G;G)
Alt rs121908487(G;G)
Reference Rs121908487(A;A)
Significance Pathogenic
Disease Cystinuria
Variation info
Gene SLC7A9
CLNDBN Cystinuria
Reversed 1
HGVS NC_000019.9:g.33353033T>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000006147.2,