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

rs200491579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200491579(C;T)
Make rs200491579(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position24261826
GeneTGM1
is asnp
is mentioned by
dbSNPrs200491579
dbSNP (classic)rs200491579
ClinGenrs200491579
ebirs200491579
HLIrs200491579
Exacrs200491579
Gnomadrs200491579
Varsomers200491579
LitVarrs200491579
Maprs200491579
PheGenIrs200491579
Biobankrs200491579
1000 genomesrs200491579
hgdprs200491579
ensemblrs200491579
geneviewrs200491579
scholarrs200491579
googlers200491579
pharmgkbrs200491579
gwascentralrs200491579
openSNPrs200491579
23andMers200491579
SNPshotrs200491579
SNPdbers200491579
MSV3drs200491579
GWAS Ctlgrs200491579
Max Magnitude0
ClinVar
Risk rs200491579(T;T)
Alt rs200491579(T;T)
Reference Rs200491579(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TGM1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.24731032C>T
CLNSRC
CLNACC RCV000329115.1,