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rs1064793448

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position46859499
GeneMYL3
is asnp
is mentioned by
dbSNPrs1064793448
dbSNP (old)rs1064793448
ClinGenrs1064793448
ebirs1064793448
HLIrs1064793448
Exacrs1064793448
Gnomadrs1064793448
Varsomers1064793448
LitVarrs1064793448
Maprs1064793448
PheGenIrs1064793448
Biobankrs1064793448
1000 genomesrs1064793448
hgdprs1064793448
ensemblrs1064793448
gopubmedrs1064793448
geneviewrs1064793448
scholarrs1064793448
googlers1064793448
pharmgkbrs1064793448
gwascentralrs1064793448
openSNPrs1064793448
23andMers1064793448
23andMe allrs1064793448
SNPshotrs1064793448
SNPdbers1064793448
MSV3drs1064793448
GWAS Ctlgrs1064793448
Max Magnitude0
ClinVar
Risk rs1064793448(-;-)
Alt rs1064793448(-;-)
Reference Rs1064793448(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYL3
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.46900989delG
CLNSRC
CLNACC RCV000485422.1,