Have questions? Visit https://www.reddit.com/r/SNPedia

rs188698686

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs188698686(A;G)
Make rs188698686(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132385369
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs188698686
ebirs188698686
HLIrs188698686
Exacrs188698686
Varsomers188698686
Maprs188698686
PheGenIrs188698686
hapmaprs188698686
1000 genomesrs188698686
hgdprs188698686
ensemblrs188698686
gopubmedrs188698686
geneviewrs188698686
scholarrs188698686
googlers188698686
pharmgkbrs188698686
gwascentralrs188698686
openSNPrs188698686
23andMers188698686
23andMe allrs188698686
SNP Nexus

SNPshotrs188698686
SNPdbers188698686
MSV3drs188698686
GWAS Ctlgrs188698686
Max Magnitude0
ClinVar
Risk rs188698686(G;G)
Alt rs188698686(G;G)
Reference rs188698686(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131721061A>C
CLNSRC
CLNACC RCV000186138.1,