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rs796052925

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052925(C;T)
Make rs796052925(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position40091338
GenePPT1
is asnp
is mentioned by
dbSNPrs796052925
ebirs796052925
HLIrs796052925
Exacrs796052925
Varsomers796052925
Maprs796052925
PheGenIrs796052925
hapmaprs796052925
1000 genomesrs796052925
hgdprs796052925
ensemblrs796052925
gopubmedrs796052925
geneviewrs796052925
scholarrs796052925
googlers796052925
pharmgkbrs796052925
gwascentralrs796052925
openSNPrs796052925
23andMers796052925
23andMe allrs796052925
SNP Nexus

SNPshotrs796052925
SNPdbers796052925
MSV3drs796052925
GWAS Ctlgrs796052925
Max Magnitude0
ClinVar
Risk rs796052925(T;T)
Alt rs796052925(T;T)
Reference rs796052925(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PPT1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.40557010G>A
CLNSRC
CLNACC RCV000188715.1,