Have questions? Visit https://www.reddit.com/r/SNPedia

rs765552494

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs765552494(C;T)
Make rs765552494(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102855227
GenePAH
is asnp
is mentioned by
dbSNPrs765552494
ebirs765552494
HLIrs765552494
Exacrs765552494
Varsomers765552494
Maprs765552494
PheGenIrs765552494
hapmaprs765552494
1000 genomesrs765552494
hgdprs765552494
ensemblrs765552494
gopubmedrs765552494
geneviewrs765552494
scholarrs765552494
googlers765552494
pharmgkbrs765552494
gwascentralrs765552494
openSNPrs765552494
23andMers765552494
23andMe allrs765552494
SNP Nexus

SNPshotrs765552494
SNPdbers765552494
MSV3drs765552494
GWAS Ctlgrs765552494
Max Magnitude0
ClinVar
Risk rs765552494(T;T)
Alt rs765552494(T;T)
Reference rs765552494(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.103249005C>G
CLNSRC
CLNACC RCV000186074.1,