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rs199475591

From SNPedia

Orientationminus
Geno Mag Summary
(-;G) 3 Carrier of a phenylketonuria mutation
(G;G) 0 common in clinvar


Make rs199475591(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102912822
GenePAH
is asnp
is mentioned by
dbSNPrs199475591
ebirs199475591
HLIrs199475591
Exacrs199475591
Varsomers199475591
Maprs199475591
PheGenIrs199475591
hapmaprs199475591
1000 genomesrs199475591
hgdprs199475591
ensemblrs199475591
gopubmedrs199475591
geneviewrs199475591
scholarrs199475591
googlers199475591
pharmgkbrs199475591
gwascentralrs199475591
openSNPrs199475591
23andMers199475591
23andMe allrs199475591
SNP Nexus

SNPshotrs199475591
SNPdbers199475591
MSV3drs199475591
GWAS Ctlgrs199475591
Max Magnitude3
ClinVar
Risk rs199475591(;)
Alt rs199475591(;)
Reference rs199475591(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103306600delC
CLNSRC
CLNACC RCV000088837.1,