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rs796052923

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052923(A;A)
Make rs796052923(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position40092397
GenePPT1
is asnp
is mentioned by
dbSNPrs796052923
ebirs796052923
HLIrs796052923
Exacrs796052923
Varsomers796052923
Maprs796052923
PheGenIrs796052923
hapmaprs796052923
1000 genomesrs796052923
hgdprs796052923
ensemblrs796052923
gopubmedrs796052923
geneviewrs796052923
scholarrs796052923
googlers796052923
pharmgkbrs796052923
gwascentralrs796052923
openSNPrs796052923
23andMers796052923
23andMe allrs796052923
SNP Nexus

SNPshotrs796052923
SNPdbers796052923
MSV3drs796052923
GWAS Ctlgrs796052923
Max Magnitude0
ClinVar
Risk rs796052923(A;A)
Alt rs796052923(A;A)
Reference rs796052923(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PPT1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.40558069C>T
CLNSRC
CLNACC RCV000188710.2,