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rs727503254

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503254(A;A)
Make rs727503254(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424770
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503254
ebirs727503254
HLIrs727503254
Exacrs727503254
Varsomers727503254
Maprs727503254
PheGenIrs727503254
hapmaprs727503254
1000 genomesrs727503254
hgdprs727503254
ensemblrs727503254
gopubmedrs727503254
geneviewrs727503254
scholarrs727503254
googlers727503254
pharmgkbrs727503254
gwascentralrs727503254
openSNPrs727503254
23andMers727503254
23andMe allrs727503254
SNP Nexus

SNPshotrs727503254
SNPdbers727503254
MSV3drs727503254
GWAS Ctlgrs727503254
Max Magnitude0
ClinVar
Risk rs727503254(A,T;A,T)
Alt rs727503254(A,T;A,T)
Reference rs727503254(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23893979G>A; NC_000014.8:g.23893979G>T
CLNSRC
CLNACC RCV000154380.2, RCV000151259.2,