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rs186476316

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs186476316(C;T)
Make rs186476316(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position119027757
GeneSLC37A4
is asnp
is mentioned by
dbSNPrs186476316
ebirs186476316
HLIrs186476316
Exacrs186476316
Varsomers186476316
Maprs186476316
PheGenIrs186476316
hapmaprs186476316
1000 genomesrs186476316
hgdprs186476316
ensemblrs186476316
gopubmedrs186476316
geneviewrs186476316
scholarrs186476316
googlers186476316
pharmgkbrs186476316
gwascentralrs186476316
openSNPrs186476316
23andMers186476316
23andMe allrs186476316
SNP Nexus

SNPshotrs186476316
SNPdbers186476316
MSV3drs186476316
GWAS Ctlgrs186476316
Max Magnitude0
ClinVar
Risk rs186476316(T;T)
Alt rs186476316(T;T)
Reference rs186476316(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC37A4
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118898467C>T
CLNSRC
CLNACC RCV000199219.2,