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rs727504311

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504311(A;G)
Make rs727504311(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424905
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504311
ebirs727504311
HLIrs727504311
Exacrs727504311
Varsomers727504311
Maprs727504311
PheGenIrs727504311
hapmaprs727504311
1000 genomesrs727504311
hgdprs727504311
ensemblrs727504311
gopubmedrs727504311
geneviewrs727504311
scholarrs727504311
googlers727504311
pharmgkbrs727504311
gwascentralrs727504311
openSNPrs727504311
23andMers727504311
23andMe allrs727504311
SNP Nexus

SNPshotrs727504311
SNPdbers727504311
MSV3drs727504311
GWAS Ctlgrs727504311
Max Magnitude0
ClinVar
Risk rs727504311(G;G)
Alt rs727504311(G;G)
Reference rs727504311(A;A)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYH7
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23894114T>C
CLNSRC
CLNACC RCV000154375.2, RCV000158548.2,