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rs1057520732

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520732(A;A)
Make rs1057520732(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position102851698
GenePAH
is asnp
is mentioned by
dbSNPrs1057520732
dbSNP (classic)rs1057520732
ClinGenrs1057520732
ebirs1057520732
HLIrs1057520732
Exacrs1057520732
Gnomadrs1057520732
Varsomers1057520732
LitVarrs1057520732
Maprs1057520732
PheGenIrs1057520732
Biobankrs1057520732
1000 genomesrs1057520732
hgdprs1057520732
ensemblrs1057520732
geneviewrs1057520732
scholarrs1057520732
googlers1057520732
pharmgkbrs1057520732
gwascentralrs1057520732
openSNPrs1057520732
23andMers1057520732
23andMe allrs1057520732
SNPshotrs1057520732
SNPdbers1057520732
MSV3drs1057520732
GWAS Ctlgrs1057520732
Max Magnitude0
ClinVar
Risk rs1057520732(A;A)
Alt rs1057520732(A;A)
Reference Rs1057520732(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103245476G>T
CLNSRC
CLNACC RCV000436688.1,