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rs756564767

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756564767(A;A)
Make rs756564767(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position6617627
GeneTPP1
is asnp
is mentioned by
dbSNPrs756564767
ebirs756564767
HLIrs756564767
Exacrs756564767
Varsomers756564767
Maprs756564767
PheGenIrs756564767
hapmaprs756564767
1000 genomesrs756564767
hgdprs756564767
ensemblrs756564767
gopubmedrs756564767
geneviewrs756564767
scholarrs756564767
googlers756564767
pharmgkbrs756564767
gwascentralrs756564767
openSNPrs756564767
23andMers756564767
23andMe allrs756564767
SNP Nexus

SNPshotrs756564767
SNPdbers756564767
MSV3drs756564767
GWAS Ctlgrs756564767
Max Magnitude0
ClinVar
Risk rs756564767(A;A)
Alt rs756564767(A;A)
Reference rs756564767(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TPP1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.6638858G>A
CLNSRC
CLNACC RCV000189759.2,