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rs796052924

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052924(A;A)
Make rs796052924(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position40092040
GenePPT1
is asnp
is mentioned by
dbSNPrs796052924
ebirs796052924
HLIrs796052924
Exacrs796052924
Varsomers796052924
Maprs796052924
PheGenIrs796052924
hapmaprs796052924
1000 genomesrs796052924
hgdprs796052924
ensemblrs796052924
gopubmedrs796052924
geneviewrs796052924
scholarrs796052924
googlers796052924
pharmgkbrs796052924
gwascentralrs796052924
openSNPrs796052924
23andMers796052924
23andMe allrs796052924
SNP Nexus

SNPshotrs796052924
SNPdbers796052924
MSV3drs796052924
GWAS Ctlgrs796052924
Max Magnitude0
ClinVar
Risk rs796052924(A;A)
Alt rs796052924(A;A)
Reference rs796052924(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PPT1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.40557712C>T
CLNSRC
CLNACC RCV000188713.2,