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rs79389353

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs79389353(C;T)
Make rs79389353(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position32862521
GeneSLC7A9
is asnp
is mentioned by
dbSNPrs79389353
ebirs79389353
HLIrs79389353
Exacrs79389353
Varsomers79389353
Maprs79389353
PheGenIrs79389353
hapmaprs79389353
1000 genomesrs79389353
hgdprs79389353
ensemblrs79389353
gopubmedrs79389353
geneviewrs79389353
scholarrs79389353
googlers79389353
pharmgkbrs79389353
gwascentralrs79389353
openSNPrs79389353
23andMers79389353
23andMe allrs79389353
SNP Nexus

SNPshotrs79389353
SNPdbers79389353
MSV3drs79389353
GWAS Ctlgrs79389353
GMAF0.001837
Max Magnitude0
OMIM604144
Desc
Variant0003
Relatedalso
ClinVar
Risk rs79389353(A,T;A,T)
Alt rs79389353(A,T;A,T)
Reference rs79389353(C;C)
Significance Other
Disease Cystinuria
Variation info
Gene SLC7A9
CLNDBN Cystinuria
Reversed 0
HGVS NC_000019.9:g.33353427C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006138.4,