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rs786205484

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205484(A;A)
Make rs786205484(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23400916
GeneMYH6
is asnp
is mentioned by
dbSNPrs786205484
ebirs786205484
HLIrs786205484
Exacrs786205484
Varsomers786205484
Maprs786205484
PheGenIrs786205484
hapmaprs786205484
1000 genomesrs786205484
hgdprs786205484
ensemblrs786205484
gopubmedrs786205484
geneviewrs786205484
scholarrs786205484
googlers786205484
pharmgkbrs786205484
gwascentralrs786205484
openSNPrs786205484
23andMers786205484
23andMe allrs786205484
SNP Nexus

SNPshotrs786205484
SNPdbers786205484
MSV3drs786205484
GWAS Ctlgrs786205484
Max Magnitude0
ClinVar
Risk rs786205484(A;A)
Alt rs786205484(A;A)
Reference rs786205484(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH6
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23870125G>T
CLNSRC
CLNACC RCV000171219.1,