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

rs1057517771

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517771(A;G)
Make rs1057517771(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23432656
GeneMYH7
is asnp
is mentioned by
dbSNPrs1057517771
dbSNP (old)rs1057517771
ClinGenrs1057517771
ebirs1057517771
HLIrs1057517771
Exacrs1057517771
Gnomadrs1057517771
Varsomers1057517771
Maprs1057517771
PheGenIrs1057517771
Biobankrs1057517771
1000 genomesrs1057517771
hgdprs1057517771
ensemblrs1057517771
gopubmedrs1057517771
geneviewrs1057517771
scholarrs1057517771
googlers1057517771
pharmgkbrs1057517771
gwascentralrs1057517771
openSNPrs1057517771
23andMers1057517771
23andMe allrs1057517771
SNPshotrs1057517771
SNPdbers1057517771
MSV3drs1057517771
GWAS Ctlgrs1057517771
Max Magnitude0
ClinVar
Risk rs1057517771(G;G)
Alt rs1057517771(G;G)
Reference Rs1057517771(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23901865T>C
CLNSRC
CLNACC RCV000413559.1,