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rs1085307959

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome14
Position23429783
GeneMYH7
is asnp
is mentioned by
dbSNPrs1085307959
dbSNP (old)rs1085307959
ClinGenrs1085307959
ebirs1085307959
HLIrs1085307959
Exacrs1085307959
Gnomadrs1085307959
Varsomers1085307959
Maprs1085307959
PheGenIrs1085307959
Biobankrs1085307959
1000 genomesrs1085307959
hgdprs1085307959
ensemblrs1085307959
gopubmedrs1085307959
geneviewrs1085307959
scholarrs1085307959
googlers1085307959
pharmgkbrs1085307959
gwascentralrs1085307959
openSNPrs1085307959
23andMers1085307959
23andMe allrs1085307959
SNPshotrs1085307959
SNPdbers1085307959
MSV3drs1085307959
GWAS Ctlgrs1085307959
Max Magnitude0
ClinVar
Risk rs1085307959(A;A)
Alt rs1085307959(A;A)
Reference Rs1085307959(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23898992C>T
CLNSRC
CLNACC RCV000490207.1,