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rs121908888

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908888(A;G)
Make rs121908888(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132384281
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs121908888
ebirs121908888
HLIrs121908888
Exacrs121908888
Varsomers121908888
Maprs121908888
PheGenIrs121908888
hapmaprs121908888
1000 genomesrs121908888
hgdprs121908888
ensemblrs121908888
gopubmedrs121908888
geneviewrs121908888
scholarrs121908888
googlers121908888
pharmgkbrs121908888
gwascentralrs121908888
openSNPrs121908888
23andMers121908888
23andMe allrs121908888
SNP Nexus

SNPshotrs121908888
SNPdbers121908888
MSV3drs121908888
GWAS Ctlgrs121908888
Merged fromRs28939705
Max Magnitude0
OMIM603377
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121908888(G;G)
Alt rs121908888(G;G)
Reference rs121908888(A;A)
Significance Pathogenic
Disease Renal carnitine transport defect not provided
Variation info
Gene SLC22A5
CLNDBN Renal carnitine transport defect not provided
Reversed 0
HGVS NC_000005.9:g.131719973A>G
CLNSRC ARUP SLC22A5 OMIM Allelic Variant
CLNACC RCV000006789.4, RCV000186136.1,