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rs1057518297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518297(C;T)
Make rs1057518297(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132390889
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs1057518297
dbSNP (old)rs1057518297
ClinGenrs1057518297
ebirs1057518297
HLIrs1057518297
Exacrs1057518297
Gnomadrs1057518297
Varsomers1057518297
Maprs1057518297
PheGenIrs1057518297
Biobankrs1057518297
1000 genomesrs1057518297
hgdprs1057518297
ensemblrs1057518297
gopubmedrs1057518297
geneviewrs1057518297
scholarrs1057518297
googlers1057518297
pharmgkbrs1057518297
gwascentralrs1057518297
openSNPrs1057518297
23andMers1057518297
23andMe allrs1057518297
SNPshotrs1057518297
SNPdbers1057518297
MSV3drs1057518297
GWAS Ctlgrs1057518297
Max Magnitude0
ClinVar
Risk rs1057518297(T;T)
Alt rs1057518297(T;T)
Reference Rs1057518297(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131726581C>T
CLNSRC
CLNACC RCV000414129.1,