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

rs1057520814

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520814(A;A)
Make rs1057520814(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23425759
GeneMYH7
is asnp
is mentioned by
dbSNPrs1057520814
dbSNP (classic)rs1057520814
ClinGenrs1057520814
ebirs1057520814
HLIrs1057520814
Exacrs1057520814
Gnomadrs1057520814
Varsomers1057520814
LitVarrs1057520814
Maprs1057520814
PheGenIrs1057520814
Biobankrs1057520814
1000 genomesrs1057520814
hgdprs1057520814
ensemblrs1057520814
geneviewrs1057520814
scholarrs1057520814
googlers1057520814
pharmgkbrs1057520814
gwascentralrs1057520814
openSNPrs1057520814
23andMers1057520814
23andMe allrs1057520814
SNPshotrs1057520814
SNPdbers1057520814
MSV3drs1057520814
GWAS Ctlgrs1057520814
Max Magnitude0
ClinVar
Risk rs1057520814(A;A)
Alt rs1057520814(A;A)
Reference Rs1057520814(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894968C>T
CLNSRC
CLNACC RCV000429053.1,