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rs1045644394

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132370174
GeneLOC553103, SLC22A5
is asnp
is mentioned by
dbSNPrs1045644394
dbSNP (old)rs1045644394
ClinGenrs1045644394
ebirs1045644394
HLIrs1045644394
Exacrs1045644394
Gnomadrs1045644394
Varsomers1045644394
Maprs1045644394
PheGenIrs1045644394
Biobankrs1045644394
1000 genomesrs1045644394
hgdprs1045644394
ensemblrs1045644394
gopubmedrs1045644394
geneviewrs1045644394
scholarrs1045644394
googlers1045644394
pharmgkbrs1045644394
gwascentralrs1045644394
openSNPrs1045644394
23andMers1045644394
23andMe allrs1045644394
SNPshotrs1045644394
SNPdbers1045644394
MSV3drs1045644394
GWAS Ctlgrs1045644394
Max Magnitude0
ClinVar
Risk rs1045644394(T;T)
Alt rs1045644394(T;T)
Reference Rs1045644394(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC553103 SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131705866C>T
CLNSRC
CLNACC RCV000481536.1,