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rs730880888

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs730880888(AA;AA)
Make rs730880888(AA;TC)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424781
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880888
ebirs730880888
HLIrs730880888
Exacrs730880888
Varsomers730880888
Maprs730880888
PheGenIrs730880888
hapmaprs730880888
1000 genomesrs730880888
hgdprs730880888
ensemblrs730880888
gopubmedrs730880888
geneviewrs730880888
scholarrs730880888
googlers730880888
pharmgkbrs730880888
gwascentralrs730880888
openSNPrs730880888
23andMers730880888
23andMe allrs730880888
SNP Nexus

SNPshotrs730880888
SNPdbers730880888
MSV3drs730880888
GWAS Ctlgrs730880888
Max Magnitude0
ClinVar
Risk rs730880888(AA;AA)
Alt rs730880888(AA;AA)
Reference rs730880888(TC;TC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893990_23893991delGAinsTT
CLNSRC
CLNACC RCV000158829.2,