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rs772153760

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772153760(C;T)
Make rs772153760(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position55679786
GenePNPT1
is asnp
is mentioned by
dbSNPrs772153760
ebirs772153760
HLIrs772153760
Exacrs772153760
Varsomers772153760
Maprs772153760
PheGenIrs772153760
hapmaprs772153760
1000 genomesrs772153760
hgdprs772153760
ensemblrs772153760
gopubmedrs772153760
geneviewrs772153760
scholarrs772153760
googlers772153760
pharmgkbrs772153760
gwascentralrs772153760
openSNPrs772153760
23andMers772153760
23andMe allrs772153760
SNP Nexus

SNPshotrs772153760
SNPdbers772153760
MSV3drs772153760
GWAS Ctlgrs772153760
Max Magnitude0
ClinVar
Risk rs772153760(T;T)
Alt rs772153760(T;T)
Reference rs772153760(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNPT1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.55906921C>T
CLNSRC
CLNACC RCV000195523.2,