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rs1035033641

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position6615257
GeneTPP1
is asnp
is mentioned by
dbSNPrs1035033641
dbSNP (old)rs1035033641
ClinGenrs1035033641
ebirs1035033641
HLIrs1035033641
Exacrs1035033641
Gnomadrs1035033641
Varsomers1035033641
LitVarrs1035033641
Maprs1035033641
PheGenIrs1035033641
Biobankrs1035033641
1000 genomesrs1035033641
hgdprs1035033641
ensemblrs1035033641
gopubmedrs1035033641
geneviewrs1035033641
scholarrs1035033641
googlers1035033641
pharmgkbrs1035033641
gwascentralrs1035033641
openSNPrs1035033641
23andMers1035033641
23andMe allrs1035033641
SNPshotrs1035033641
SNPdbers1035033641
MSV3drs1035033641
GWAS Ctlgrs1035033641
Max Magnitude0
ClinVar
Risk rs1035033641(A;A)
Alt rs1035033641(A;A)
Reference Rs1035033641(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.6636488G>A
CLNSRC
CLNACC RCV000489192.1,