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rs1057519221

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519221(A;A)
Make rs1057519221(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23432796
GeneMYH7
is asnp
is mentioned by
dbSNPrs1057519221
dbSNP (old)rs1057519221
ClinGenrs1057519221
ebirs1057519221
HLIrs1057519221
Exacrs1057519221
Gnomadrs1057519221
Varsomers1057519221
Maprs1057519221
PheGenIrs1057519221
Biobankrs1057519221
1000 genomesrs1057519221
hgdprs1057519221
ensemblrs1057519221
gopubmedrs1057519221
geneviewrs1057519221
scholarrs1057519221
googlers1057519221
pharmgkbrs1057519221
gwascentralrs1057519221
openSNPrs1057519221
23andMers1057519221
23andMe allrs1057519221
SNPshotrs1057519221
SNPdbers1057519221
MSV3drs1057519221
GWAS Ctlgrs1057519221
Max Magnitude0
ClinVar
Risk rs1057519221(A;A)
Alt rs1057519221(A;A)
Reference Rs1057519221(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23902005C>T
CLNSRC
CLNACC RCV000415886.1,