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rs767310806

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs767310806(G;G)
Make rs767310806(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position55654942
GenePNPT1
is asnp
is mentioned by
dbSNPrs767310806
ebirs767310806
HLIrs767310806
Exacrs767310806
Varsomers767310806
Maprs767310806
PheGenIrs767310806
hapmaprs767310806
1000 genomesrs767310806
hgdprs767310806
ensemblrs767310806
gopubmedrs767310806
geneviewrs767310806
scholarrs767310806
googlers767310806
pharmgkbrs767310806
gwascentralrs767310806
openSNPrs767310806
23andMers767310806
23andMe allrs767310806
SNP Nexus

SNPshotrs767310806
SNPdbers767310806
MSV3drs767310806
GWAS Ctlgrs767310806
Max Magnitude0
ClinVar
Risk rs767310806(G;G)
Alt rs767310806(G;G)
Reference rs767310806(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PNPT1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.55882077T>C
CLNSRC
CLNACC RCV000195745.1,