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rs387907097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907097(G;G)
Make rs387907097(G;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position2417445
GeneTGM6
is asnp
is mentioned by
dbSNPrs387907097
ebirs387907097
HLIrs387907097
Exacrs387907097
Varsomers387907097
Maprs387907097
PheGenIrs387907097
hapmaprs387907097
1000 genomesrs387907097
hgdprs387907097
ensemblrs387907097
gopubmedrs387907097
geneviewrs387907097
scholarrs387907097
googlers387907097
pharmgkbrs387907097
gwascentralrs387907097
openSNPrs387907097
23andMers387907097
23andMe allrs387907097
SNP Nexus

SNPshotrs387907097
SNPdbers387907097
MSV3drs387907097
GWAS Ctlgrs387907097
Max Magnitude0
ClinVar
Risk rs387907097(G;G)
Alt rs387907097(G;G)
Reference rs387907097(T;T)
Significance Pathogenic
Disease Spinocerebellar ataxia 35 Acute myeloid leukemia
Variation info
Gene TGM6
CLNDBN Spinocerebellar ataxia 35 Acute myeloid leukemia
Reversed 0
HGVS NC_000020.10:g.2398091T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024080.2, RCV000077795.1,