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

rs1057518398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518398(G;T)
Make rs1057518398(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position10539927
GeneMYHAS, MYH2
is asnp
is mentioned by
dbSNPrs1057518398
dbSNP (old)rs1057518398
ClinGenrs1057518398
ebirs1057518398
HLIrs1057518398
Exacrs1057518398
Gnomadrs1057518398
Varsomers1057518398
LitVarrs1057518398
Maprs1057518398
PheGenIrs1057518398
Biobankrs1057518398
1000 genomesrs1057518398
hgdprs1057518398
ensemblrs1057518398
gopubmedrs1057518398
geneviewrs1057518398
scholarrs1057518398
googlers1057518398
pharmgkbrs1057518398
gwascentralrs1057518398
openSNPrs1057518398
23andMers1057518398
23andMe allrs1057518398
SNPshotrs1057518398
SNPdbers1057518398
MSV3drs1057518398
GWAS Ctlgrs1057518398
Max Magnitude0
ClinVar
Risk rs1057518398(T;T)
Alt rs1057518398(T;T)
Reference Rs1057518398(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH2 MYHAS
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.10443244C>A
CLNSRC
CLNACC RCV000413618.1,