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

rs727504261

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504261(A;G)
Make rs727504261(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424121
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504261
ebirs727504261
HLIrs727504261
Exacrs727504261
Varsomers727504261
Maprs727504261
PheGenIrs727504261
hapmaprs727504261
1000 genomesrs727504261
hgdprs727504261
ensemblrs727504261
gopubmedrs727504261
geneviewrs727504261
scholarrs727504261
googlers727504261
pharmgkbrs727504261
gwascentralrs727504261
openSNPrs727504261
23andMers727504261
23andMe allrs727504261
SNP Nexus

SNPshotrs727504261
SNPdbers727504261
MSV3drs727504261
GWAS Ctlgrs727504261
Max Magnitude0
ClinVar
Risk rs727504261(G;G)
Alt rs727504261(G;G)
Reference rs727504261(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23893330T>C
CLNSRC
CLNACC RCV000154244.2,