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

rs1085308025

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome14
Position23415195
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs1085308025
dbSNP (old)rs1085308025
ClinGenrs1085308025
ebirs1085308025
HLIrs1085308025
Exacrs1085308025
Gnomadrs1085308025
Varsomers1085308025
Maprs1085308025
PheGenIrs1085308025
Biobankrs1085308025
1000 genomesrs1085308025
hgdprs1085308025
ensemblrs1085308025
gopubmedrs1085308025
geneviewrs1085308025
scholarrs1085308025
googlers1085308025
pharmgkbrs1085308025
gwascentralrs1085308025
openSNPrs1085308025
23andMers1085308025
23andMe allrs1085308025
SNPshotrs1085308025
SNPdbers1085308025
MSV3drs1085308025
GWAS Ctlgrs1085308025
Max Magnitude0
ClinVar
Risk rs1085308025(C;C)
Alt rs1085308025(C;C)
Reference Rs1085308025(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23884404C>G
CLNSRC
CLNACC RCV000489988.1,