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rs199475605

From SNPedia

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


Make rs199475605(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102877502
GenePAH
is asnp
is mentioned by
dbSNPrs199475605
ebirs199475605
HLIrs199475605
Exacrs199475605
Varsomers199475605
Maprs199475605
PheGenIrs199475605
hapmaprs199475605
1000 genomesrs199475605
hgdprs199475605
ensemblrs199475605
gopubmedrs199475605
geneviewrs199475605
scholarrs199475605
googlers199475605
pharmgkbrs199475605
gwascentralrs199475605
openSNPrs199475605
23andMers199475605
23andMe allrs199475605
SNP Nexus

SNPshotrs199475605
SNPdbers199475605
MSV3drs199475605
GWAS Ctlgrs199475605
Max Magnitude3
ClinVar
Risk rs199475605(;)
Alt rs199475605(;)
Reference rs199475605(ATCA;ATCA)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103271280_103271283delTGAT
CLNSRC
CLNACC RCV000088910.1,