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rs1060499787

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499787(C;C)
Make rs1060499787(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position32860605
GeneSLC7A9
is asnp
is mentioned by
dbSNPrs1060499787
dbSNP (classic)rs1060499787
ClinGenrs1060499787
ebirs1060499787
HLIrs1060499787
Exacrs1060499787
Gnomadrs1060499787
Varsomers1060499787
LitVarrs1060499787
Maprs1060499787
PheGenIrs1060499787
Biobankrs1060499787
1000 genomesrs1060499787
hgdprs1060499787
ensemblrs1060499787
geneviewrs1060499787
scholarrs1060499787
googlers1060499787
pharmgkbrs1060499787
gwascentralrs1060499787
openSNPrs1060499787
23andMers1060499787
23andMe allrs1060499787
SNPshotrs1060499787
SNPdbers1060499787
MSV3drs1060499787
GWAS Ctlgrs1060499787
Max Magnitude0
ClinVar
Risk rs1060499787(C;C)
Alt rs1060499787(C;C)
Reference Rs1060499787(G;G)
Significance Probable-Pathogenic
Disease Cystinuria
Variation info
Gene SLC7A9
CLNDBN Cystinuria
Reversed 1
HGVS NC_000019.9:g.33351511C>G
CLNSRC
CLNACC RCV000454228.1,