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rs1057523846

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523846(A;A)
Make rs1057523846(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position75844896
GeneMYO6
is asnp
is mentioned by
dbSNPrs1057523846
dbSNP (old)rs1057523846
ClinGenrs1057523846
ebirs1057523846
HLIrs1057523846
Exacrs1057523846
Gnomadrs1057523846
Varsomers1057523846
Maprs1057523846
PheGenIrs1057523846
Biobankrs1057523846
1000 genomesrs1057523846
hgdprs1057523846
ensemblrs1057523846
gopubmedrs1057523846
geneviewrs1057523846
scholarrs1057523846
googlers1057523846
pharmgkbrs1057523846
gwascentralrs1057523846
openSNPrs1057523846
23andMers1057523846
23andMe allrs1057523846
SNPshotrs1057523846
SNPdbers1057523846
MSV3drs1057523846
GWAS Ctlgrs1057523846
Max Magnitude0
ClinVar
Risk rs1057523846(A;A)
Alt rs1057523846(A;A)
Reference Rs1057523846(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYO6
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.76554613G>A
CLNSRC
CLNACC RCV000422184.1,