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rs746085696

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746085696(C;T)
Make rs746085696(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position6619191
GeneTPP1
is asnp
is mentioned by
dbSNPrs746085696
ebirs746085696
HLIrs746085696
Exacrs746085696
Varsomers746085696
Maprs746085696
PheGenIrs746085696
hapmaprs746085696
1000 genomesrs746085696
hgdprs746085696
ensemblrs746085696
gopubmedrs746085696
geneviewrs746085696
scholarrs746085696
googlers746085696
pharmgkbrs746085696
gwascentralrs746085696
openSNPrs746085696
23andMers746085696
23andMe allrs746085696
SNP Nexus

SNPshotrs746085696
SNPdbers746085696
MSV3drs746085696
GWAS Ctlgrs746085696
Max Magnitude0
ClinVar
Risk rs746085696(T;T)
Alt rs746085696(T;T)
Reference rs746085696(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TPP1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.6640422C>G
CLNSRC
CLNACC RCV000189799.1,