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rs730880761

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880761(A;T)
Make rs730880761(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424025
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880761
ebirs730880761
HLIrs730880761
Exacrs730880761
Varsomers730880761
Maprs730880761
PheGenIrs730880761
hapmaprs730880761
1000 genomesrs730880761
hgdprs730880761
ensemblrs730880761
gopubmedrs730880761
geneviewrs730880761
scholarrs730880761
googlers730880761
pharmgkbrs730880761
gwascentralrs730880761
openSNPrs730880761
23andMers730880761
23andMe allrs730880761
SNP Nexus

SNPshotrs730880761
SNPdbers730880761
MSV3drs730880761
GWAS Ctlgrs730880761
Max Magnitude0
ClinVar
Risk rs730880761(T;T)
Alt rs730880761(T;T)
Reference rs730880761(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893234T>A
CLNSRC
CLNACC RCV000158577.2,