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rs199475666

From SNPedia

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


Make rs199475666(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852920
GenePAH
is asnp
is mentioned by
dbSNPrs199475666
ebirs199475666
HLIrs199475666
Exacrs199475666
Varsomers199475666
Maprs199475666
PheGenIrs199475666
hapmaprs199475666
1000 genomesrs199475666
hgdprs199475666
ensemblrs199475666
gopubmedrs199475666
geneviewrs199475666
scholarrs199475666
googlers199475666
pharmgkbrs199475666
gwascentralrs199475666
openSNPrs199475666
23andMers199475666
23andMe allrs199475666
SNP Nexus

SNPshotrs199475666
SNPdbers199475666
MSV3drs199475666
GWAS Ctlgrs199475666
Max Magnitude3
ClinVar
Risk rs199475666(;)
Alt rs199475666(;)
Reference rs199475666(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246698delG
CLNSRC
CLNACC RCV000089069.1,