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rs199474705

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199474705(A;A)
Make rs199474705(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position46859502
GeneMYL3
is asnp
is mentioned by
dbSNPrs199474705
dbSNP (old)rs199474705
ClinGenrs199474705
ebirs199474705
HLIrs199474705
Exacrs199474705
Gnomadrs199474705
Varsomers199474705
LitVarrs199474705
Maprs199474705
PheGenIrs199474705
Biobankrs199474705
1000 genomesrs199474705
hgdprs199474705
ensemblrs199474705
gopubmedrs199474705
geneviewrs199474705
scholarrs199474705
googlers199474705
pharmgkbrs199474705
gwascentralrs199474705
openSNPrs199474705
23andMers199474705
23andMe allrs199474705
SNPshotrs199474705
SNPdbers199474705
MSV3drs199474705
GWAS Ctlgrs199474705
Max Magnitude0
ClinVar
Risk rs199474705(A;A)
Alt rs199474705(A;A)
Reference Rs199474705(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYL3
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.46900992C>T
CLNSRC Leiden Muscular Dystrophy pages (MYL3)
CLNACC RCV000024473.1,