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rs727504270

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504270(A;G)
Make rs727504270(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23428582
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504270
ebirs727504270
HLIrs727504270
Exacrs727504270
Varsomers727504270
Maprs727504270
PheGenIrs727504270
hapmaprs727504270
1000 genomesrs727504270
hgdprs727504270
ensemblrs727504270
gopubmedrs727504270
geneviewrs727504270
scholarrs727504270
googlers727504270
pharmgkbrs727504270
gwascentralrs727504270
openSNPrs727504270
23andMers727504270
23andMe allrs727504270
SNP Nexus

SNPshotrs727504270
SNPdbers727504270
MSV3drs727504270
GWAS Ctlgrs727504270
Max Magnitude0
ClinVar
Risk rs727504270(G;G)
Alt rs727504270(G;G)
Reference rs727504270(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23897791T>C
CLNSRC
CLNACC RCV000154260.2,