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rs786205485

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786205485(-;-)
Make rs786205485(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position24259710
GeneTGM1
is asnp
is mentioned by
dbSNPrs786205485
ebirs786205485
HLIrs786205485
Exacrs786205485
Varsomers786205485
Maprs786205485
PheGenIrs786205485
hapmaprs786205485
1000 genomesrs786205485
hgdprs786205485
ensemblrs786205485
gopubmedrs786205485
geneviewrs786205485
scholarrs786205485
googlers786205485
pharmgkbrs786205485
gwascentralrs786205485
openSNPrs786205485
23andMers786205485
23andMe allrs786205485
SNP Nexus

SNPshotrs786205485
SNPdbers786205485
MSV3drs786205485
GWAS Ctlgrs786205485
Max Magnitude0
ClinVar
Risk rs786205485(;)
Alt rs786205485(;)
Reference rs786205485(CT;CT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGM1
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.24728916_24728917delAG
CLNSRC
CLNACC RCV000171220.1,