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rs7164902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs7164902(A;A)
Make rs7164902(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position34258881
GeneSLC12A6
is asnp
is mentioned by
dbSNPrs7164902
dbSNP (classic)rs7164902
ClinGenrs7164902
ebirs7164902
HLIrs7164902
Exacrs7164902
Gnomadrs7164902
Varsomers7164902
LitVarrs7164902
Maprs7164902
PheGenIrs7164902
Biobankrs7164902
1000 genomesrs7164902
hgdprs7164902
ensemblrs7164902
geneviewrs7164902
scholarrs7164902
googlers7164902
pharmgkbrs7164902
gwascentralrs7164902
openSNPrs7164902
23andMers7164902
SNPshotrs7164902
SNPdbers7164902
MSV3drs7164902
GWAS Ctlgrs7164902
GMAF0.2704
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 21245421] Genetic Factors Underlying the Risk of Thalidomide-Related Neuropathy in Patients With Multiple Myeloma


ClinVar
Risk rs7164902(A;A)
Alt rs7164902(A;A)
Reference Rs7164902(G;G)
Significance Non-pathogenic
Disease not specified Andermann syndrome
Variation info
Gene SLC12A6
CLNDBN not specified Andermann syndrome
Reversed 0
HGVS NC_000015.9:g.34551082G>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000147488.2, RCV000271997.1,