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

rs730880914

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880914(A;A)
Make rs730880914(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415756
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880914
ebirs730880914
HLIrs730880914
Exacrs730880914
Varsomers730880914
Maprs730880914
PheGenIrs730880914
hapmaprs730880914
1000 genomesrs730880914
hgdprs730880914
ensemblrs730880914
gopubmedrs730880914
geneviewrs730880914
scholarrs730880914
googlers730880914
pharmgkbrs730880914
gwascentralrs730880914
openSNPrs730880914
23andMers730880914
23andMe allrs730880914
SNP Nexus

SNPshotrs730880914
SNPdbers730880914
MSV3drs730880914
GWAS Ctlgrs730880914
Max Magnitude0
ClinVar
Risk rs730880914(A;A)
Alt rs730880914(A;A)
Reference rs730880914(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23884965C>T
CLNSRC
CLNACC RCV000158869.2,