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rs76542238

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 Carrier of a phenylketonuria mutation
Make rs76542238(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102839194
GenePAH
is asnp
is mentioned by
dbSNPrs76542238
ebirs76542238
HLIrs76542238
Exacrs76542238
Varsomers76542238
Maprs76542238
PheGenIrs76542238
hapmaprs76542238
1000 genomesrs76542238
hgdprs76542238
ensemblrs76542238
gopubmedrs76542238
geneviewrs76542238
scholarrs76542238
googlers76542238
pharmgkbrs76542238
gwascentralrs76542238
openSNPrs76542238
23andMers76542238
23andMe allrs76542238
SNP Nexus

SNPshotrs76542238
SNPdbers76542238
MSV3drs76542238
GWAS Ctlgrs76542238
Max Magnitude3
ClinVar
Risk rs76542238(T;T)
Alt rs76542238(T;T)
Reference rs76542238(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.103232972G>T
CLNSRC
CLNACC RCV000088834.1,