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rs779093807

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs779093807(A;A)
Make rs779093807(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18166449
GeneMYO15A
is asnp
is mentioned by
dbSNPrs779093807
dbSNP (classic)rs779093807
ClinGenrs779093807
ebirs779093807
HLIrs779093807
Exacrs779093807
Gnomadrs779093807
Varsomers779093807
LitVarrs779093807
Maprs779093807
PheGenIrs779093807
Biobankrs779093807
1000 genomesrs779093807
hgdprs779093807
ensemblrs779093807
geneviewrs779093807
scholarrs779093807
googlers779093807
pharmgkbrs779093807
gwascentralrs779093807
openSNPrs779093807
23andMers779093807
SNPshotrs779093807
SNPdbers779093807
MSV3drs779093807
GWAS Ctlgrs779093807
Max Magnitude0
ClinVar
Risk rs779093807(A;A) rs779093807(T;T)
Alt rs779093807(A;A) rs779093807(T;T)
Reference Rs779093807(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYO15A
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.18069763G>A
CLNSRC
CLNACC RCV000433268.1,