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

rs144321381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144321381(G;T)
Make rs144321381(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position10412667
GeneMYHAS, MYH8
is asnp
is mentioned by
dbSNPrs144321381
ebirs144321381
HLIrs144321381
Exacrs144321381
Varsomers144321381
Maprs144321381
PheGenIrs144321381
hapmaprs144321381
1000 genomesrs144321381
hgdprs144321381
ensemblrs144321381
gopubmedrs144321381
geneviewrs144321381
scholarrs144321381
googlers144321381
pharmgkbrs144321381
gwascentralrs144321381
openSNPrs144321381
23andMers144321381
23andMe allrs144321381
SNP Nexus

SNPshotrs144321381
SNPdbers144321381
MSV3drs144321381
GWAS Ctlgrs144321381
Max Magnitude0
ClinVar
Risk rs144321381(T;T)
Alt rs144321381(T;T)
Reference rs144321381(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYHAS MYH8
CLNDBN not specified
Reversed 0
HGVS NC_000017.10:g.10315984G>T
CLNSRC ClinVar
CLNACC RCV000117683.2,