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rs1064793207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Chromosome20
Position31826885
GeneMYLK2
is asnp
is mentioned by
dbSNPrs1064793207
dbSNP (old)rs1064793207
ClinGenrs1064793207
ebirs1064793207
HLIrs1064793207
Exacrs1064793207
Gnomadrs1064793207
Varsomers1064793207
LitVarrs1064793207
Maprs1064793207
PheGenIrs1064793207
Biobankrs1064793207
1000 genomesrs1064793207
hgdprs1064793207
ensemblrs1064793207
gopubmedrs1064793207
geneviewrs1064793207
scholarrs1064793207
googlers1064793207
pharmgkbrs1064793207
gwascentralrs1064793207
openSNPrs1064793207
23andMers1064793207
23andMe allrs1064793207
SNPshotrs1064793207
SNPdbers1064793207
MSV3drs1064793207
GWAS Ctlgrs1064793207
Max Magnitude0
ClinVar
Risk rs1064793207(-;-)
Alt rs1064793207(-;-)
Reference Rs1064793207(TG;TG)
Significance Probable-Pathogenic
Disease Cardiomyopathy not provided
Variation info
Gene MYLK2
CLNDBN Cardiomyopathy not provided
Reversed 0
HGVS NC_000020.10:g.30414690_30414691delTG
CLNSRC
CLNACC RCV000183562.1, RCV000481664.1,