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rs63186960

From SNPedia

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


Make rs63186960(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102840516
GenePAH
is asnp
is mentioned by
dbSNPrs63186960
ebirs63186960
HLIrs63186960
Exacrs63186960
Varsomers63186960
Maprs63186960
PheGenIrs63186960
hapmaprs63186960
1000 genomesrs63186960
hgdprs63186960
ensemblrs63186960
gopubmedrs63186960
geneviewrs63186960
scholarrs63186960
googlers63186960
pharmgkbrs63186960
gwascentralrs63186960
openSNPrs63186960
23andMers63186960
23andMe allrs63186960
SNP Nexus

SNPshotrs63186960
SNPdbers63186960
MSV3drs63186960
GWAS Ctlgrs63186960
Max Magnitude3
ClinVar
Risk rs63186960(;)
Alt rs63186960(;)
Reference rs63186960(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103234294delC
CLNSRC
CLNACC RCV000088798.1,