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

rs199475641

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs199475641(-;-)
Make rs199475641(-;A)
Make rs199475641(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102839178
GenePAH
is asnp
is mentioned by
dbSNPrs199475641
ebirs199475641
HLIrs199475641
Exacrs199475641
Varsomers199475641
Maprs199475641
PheGenIrs199475641
hapmaprs199475641
1000 genomesrs199475641
hgdprs199475641
ensemblrs199475641
gopubmedrs199475641
geneviewrs199475641
scholarrs199475641
googlers199475641
pharmgkbrs199475641
gwascentralrs199475641
openSNPrs199475641
23andMers199475641
23andMe allrs199475641
SNP Nexus

SNPshotrs199475641
SNPdbers199475641
MSV3drs199475641
GWAS Ctlgrs199475641
Max Magnitude0
ClinVar
Risk rs199475641(A;A)
Alt rs199475641(A;A)
Reference rs199475641(;)
Significance Probable-Pathogenic
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103232957dupT
CLNSRC
CLNACC RCV000088835.1, RCV000169511.1,