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

rs730880875

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880875(A;G)
Make rs730880875(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23428601
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880875
ebirs730880875
HLIrs730880875
Exacrs730880875
Varsomers730880875
Maprs730880875
PheGenIrs730880875
hapmaprs730880875
1000 genomesrs730880875
hgdprs730880875
ensemblrs730880875
gopubmedrs730880875
geneviewrs730880875
scholarrs730880875
googlers730880875
pharmgkbrs730880875
gwascentralrs730880875
openSNPrs730880875
23andMers730880875
23andMe allrs730880875
SNP Nexus

SNPshotrs730880875
SNPdbers730880875
MSV3drs730880875
GWAS Ctlgrs730880875
Max Magnitude0
ClinVar
Risk rs730880875(G;G)
Alt rs730880875(G;G)
Reference rs730880875(A;A)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23897810T>C
CLNSRC
CLNACC RCV000158807.2, RCV000213209.1,