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rs74503222

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 3 Carrier of a phenylketonuria mutation
(G;G) 0 common in clinvar


Make rs74503222(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102852912
GenePAH
is asnp
is mentioned by
dbSNPrs74503222
dbSNP (classic)rs74503222
ClinGenrs74503222
ebirs74503222
HLIrs74503222
Exacrs74503222
Gnomadrs74503222
Varsomers74503222
LitVarrs74503222
Maprs74503222
PheGenIrs74503222
Biobankrs74503222
1000 genomesrs74503222
hgdprs74503222
ensemblrs74503222
geneviewrs74503222
scholarrs74503222
googlers74503222
pharmgkbrs74503222
gwascentralrs74503222
openSNPrs74503222
23andMers74503222
SNPshotrs74503222
SNPdbers74503222
MSV3drs74503222
GWAS Ctlgrs74503222
Max Magnitude3

aka c.745C>T (p.Leu249Phe)

FTDNA & MyHeritage name: VG12S8420

ClinVar
Risk rs74503222(A;A)
Alt rs74503222(A;A)
Reference Rs74503222(G;G)
Significance Pathogenic
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 0
HGVS NC_000012.11:g.103246690G>A
CLNSRC HGMD UniProtKB (protein)
CLNACC RCV000089076.3, RCV000153634.3,