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rs727504401

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504401(A;G)
Make rs727504401(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23428508
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504401
ebirs727504401
HLIrs727504401
Exacrs727504401
Varsomers727504401
Maprs727504401
PheGenIrs727504401
hapmaprs727504401
1000 genomesrs727504401
hgdprs727504401
ensemblrs727504401
gopubmedrs727504401
geneviewrs727504401
scholarrs727504401
googlers727504401
pharmgkbrs727504401
gwascentralrs727504401
openSNPrs727504401
23andMers727504401
23andMe allrs727504401
SNP Nexus

SNPshotrs727504401
SNPdbers727504401
MSV3drs727504401
GWAS Ctlgrs727504401
Max Magnitude0
ClinVar
Risk rs727504401(G;G)
Alt rs727504401(G;G)
Reference rs727504401(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23897717T>C
CLNSRC
CLNACC RCV000154578.2,