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

rs199474708

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199474708(A;G)
Make rs199474708(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46858426
GeneMYL3
is asnp
is mentioned by
dbSNPrs199474708
ebirs199474708
HLIrs199474708
Exacrs199474708
Varsomers199474708
Maprs199474708
PheGenIrs199474708
hapmaprs199474708
1000 genomesrs199474708
hgdprs199474708
ensemblrs199474708
gopubmedrs199474708
geneviewrs199474708
scholarrs199474708
googlers199474708
pharmgkbrs199474708
gwascentralrs199474708
openSNPrs199474708
23andMers199474708
23andMe allrs199474708
SNP Nexus

SNPshotrs199474708
SNPdbers199474708
MSV3drs199474708
GWAS Ctlgrs199474708
Max Magnitude0
ClinVar
Risk rs199474708(G;G)
Alt rs199474708(G;G)
Reference rs199474708(A;A)
Significance Untested
Disease not provided not specified
Variation info
Gene MYL3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000003.11:g.46899916T>C
CLNSRC Leiden Muscular Dystrophy pages (MYL3)
CLNACC RCV000024470.1, RCV000036029.3,