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rs142553916

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142553916(A;A)
Make rs142553916(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position73621883
GeneSLC17A5
is asnp
is mentioned by
dbSNPrs142553916
ebirs142553916
HLIrs142553916
Exacrs142553916
Varsomers142553916
Maprs142553916
PheGenIrs142553916
hapmaprs142553916
1000 genomesrs142553916
hgdprs142553916
ensemblrs142553916
gopubmedrs142553916
geneviewrs142553916
scholarrs142553916
googlers142553916
pharmgkbrs142553916
gwascentralrs142553916
openSNPrs142553916
23andMers142553916
23andMe allrs142553916
SNP Nexus

SNPshotrs142553916
SNPdbers142553916
MSV3drs142553916
GWAS Ctlgrs142553916
Max Magnitude0
ClinVar
Risk rs142553916(A;A)
Alt rs142553916(A;A)
Reference rs142553916(G;G)
Significance Other
Disease not provided
Variation info
Gene SLC17A5
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.74331606G>A
CLNSRC
CLNACC RCV000171400.2,