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rs786205659

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205659(-;-)
Make rs786205659(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position69225352
GeneTJP2
is asnp
is mentioned by
dbSNPrs786205659
ebirs786205659
HLIrs786205659
Exacrs786205659
Varsomers786205659
Maprs786205659
PheGenIrs786205659
hapmaprs786205659
1000 genomesrs786205659
hgdprs786205659
ensemblrs786205659
gopubmedrs786205659
geneviewrs786205659
scholarrs786205659
googlers786205659
pharmgkbrs786205659
gwascentralrs786205659
openSNPrs786205659
23andMers786205659
23andMe allrs786205659
SNP Nexus

SNPshotrs786205659
SNPdbers786205659
MSV3drs786205659
GWAS Ctlgrs786205659
Max Magnitude0
ClinVar
Risk rs786205659(;)
Alt rs786205659(;)
Reference rs786205659(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TJP2
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.71840268delG
CLNSRC
CLNACC RCV000171538.1,