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rs62508730

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62508730(A;A)
Make rs62508730(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102852935
GenePAH
is asnp
is mentioned by
dbSNPrs62508730
ebirs62508730
HLIrs62508730
Exacrs62508730
Varsomers62508730
Maprs62508730
PheGenIrs62508730
hapmaprs62508730
1000 genomesrs62508730
hgdprs62508730
ensemblrs62508730
gopubmedrs62508730
geneviewrs62508730
scholarrs62508730
googlers62508730
pharmgkbrs62508730
gwascentralrs62508730
openSNPrs62508730
23andMers62508730
23andMe allrs62508730
SNP Nexus

SNPshotrs62508730
SNPdbers62508730
MSV3drs62508730
GWAS Ctlgrs62508730
Max Magnitude0
ClinVar
Risk rs62508730(A,T;A,T)
Alt rs62508730(A,T;A,T)
Reference rs62508730(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246713C>A; NC_000012.11:g.103246713C>T
CLNSRC
CLNACC RCV000089056.1, RCV000089055.3,