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rs185551386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs185551386(A;A)
Make rs185551386(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132385355
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs185551386
dbSNP (classic)rs185551386
ClinGenrs185551386
ebirs185551386
HLIrs185551386
Exacrs185551386
Gnomadrs185551386
Varsomers185551386
LitVarrs185551386
Maprs185551386
PheGenIrs185551386
Biobankrs185551386
1000 genomesrs185551386
hgdprs185551386
ensemblrs185551386
geneviewrs185551386
scholarrs185551386
googlers185551386
pharmgkbrs185551386
gwascentralrs185551386
openSNPrs185551386
23andMers185551386
23andMe allrs185551386
SNPshotrs185551386
SNPdbers185551386
MSV3drs185551386
GWAS Ctlgrs185551386
Max Magnitude0
ClinVar
Risk rs185551386(A;A)
Alt rs185551386(A;A)
Reference Rs185551386(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131721047G>A
CLNSRC
CLNACC RCV000427349.1,