Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1037293795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position102843698
GenePAH
is asnp
is mentioned by
dbSNPrs1037293795
dbSNP (old)rs1037293795
ClinGenrs1037293795
ebirs1037293795
HLIrs1037293795
Exacrs1037293795
Gnomadrs1037293795
Varsomers1037293795
Maprs1037293795
PheGenIrs1037293795
Biobankrs1037293795
1000 genomesrs1037293795
hgdprs1037293795
ensemblrs1037293795
gopubmedrs1037293795
geneviewrs1037293795
scholarrs1037293795
googlers1037293795
pharmgkbrs1037293795
gwascentralrs1037293795
openSNPrs1037293795
23andMers1037293795
23andMe allrs1037293795
SNPshotrs1037293795
SNPdbers1037293795
MSV3drs1037293795
GWAS Ctlgrs1037293795
Max Magnitude0
ClinVar
Risk rs1037293795(A;A)
Alt rs1037293795(A;A)
Reference Rs1037293795(G;G)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene
CLNDBN Phenylketonuria
Reversed 0
HGVS NC_000012.11:g.103237476G>A
CLNSRC
CLNACC RCV000409716.1,