Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205595

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205595(C;T)
Make rs786205595(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position139885900
GeneTRAPPC9
is asnp
is mentioned by
dbSNPrs786205595
ebirs786205595
HLIrs786205595
Exacrs786205595
Varsomers786205595
Maprs786205595
PheGenIrs786205595
hapmaprs786205595
1000 genomesrs786205595
hgdprs786205595
ensemblrs786205595
gopubmedrs786205595
geneviewrs786205595
scholarrs786205595
googlers786205595
pharmgkbrs786205595
gwascentralrs786205595
openSNPrs786205595
23andMers786205595
23andMe allrs786205595
SNP Nexus

SNPshotrs786205595
SNPdbers786205595
MSV3drs786205595
GWAS Ctlgrs786205595
Max Magnitude0
ClinVar
Risk rs786205595(T;T)
Alt rs786205595(T;T)
Reference rs786205595(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRAPPC9
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.140898144G>A
CLNSRC
CLNACC RCV000171421.1,