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rs786205622

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786205622(-;-)
Make rs786205622(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position123672117
GeneTCTN2
is asnp
is mentioned by
dbSNPrs786205622
ebirs786205622
HLIrs786205622
Exacrs786205622
Varsomers786205622
Maprs786205622
PheGenIrs786205622
hapmaprs786205622
1000 genomesrs786205622
hgdprs786205622
ensemblrs786205622
gopubmedrs786205622
geneviewrs786205622
scholarrs786205622
googlers786205622
pharmgkbrs786205622
gwascentralrs786205622
openSNPrs786205622
23andMers786205622
23andMe allrs786205622
SNP Nexus

SNPshotrs786205622
SNPdbers786205622
MSV3drs786205622
GWAS Ctlgrs786205622
Max Magnitude0
ClinVar
Risk rs786205622(;)
Alt rs786205622(;)
Reference rs786205622(TG;TG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCTN2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.124156664_124156665delTG
CLNSRC
CLNACC RCV000171472.1,