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rs796052017

From SNPedia

Orientationminus
Make rs796052017(CA;CA)
Make rs796052017(CA;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102852922
GenePAH
is asnp
is mentioned by
dbSNPrs796052017
ebirs796052017
HLIrs796052017
Exacrs796052017
Varsomers796052017
Maprs796052017
PheGenIrs796052017
hapmaprs796052017
1000 genomesrs796052017
hgdprs796052017
ensemblrs796052017
gopubmedrs796052017
geneviewrs796052017
scholarrs796052017
googlers796052017
pharmgkbrs796052017
gwascentralrs796052017
openSNPrs796052017
23andMers796052017
23andMe allrs796052017
SNP Nexus

SNPshotrs796052017
SNPdbers796052017
MSV3drs796052017
GWAS Ctlgrs796052017
Max Magnitude
ClinVar
Risk rs796052017(CA;CA)
Alt rs796052017(CA;CA)
Reference rs796052017(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246700_103246701delCAinsTG
CLNSRC
CLNACC RCV000186078.1,