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rs727504362

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504362(C;T)
Make rs727504362(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431619
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504362
ebirs727504362
HLIrs727504362
Exacrs727504362
Varsomers727504362
Maprs727504362
PheGenIrs727504362
hapmaprs727504362
1000 genomesrs727504362
hgdprs727504362
ensemblrs727504362
gopubmedrs727504362
geneviewrs727504362
scholarrs727504362
googlers727504362
pharmgkbrs727504362
gwascentralrs727504362
openSNPrs727504362
23andMers727504362
23andMe allrs727504362
SNP Nexus

SNPshotrs727504362
SNPdbers727504362
MSV3drs727504362
GWAS Ctlgrs727504362
Max Magnitude0
ClinVar
Risk rs727504362(T;T)
Alt rs727504362(T;T)
Reference rs727504362(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23900828G>A
CLNSRC
CLNACC RCV000154496.2,