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rs1057517774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517774(C;G)
Make rs1057517774(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77162845
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1057517774
dbSNP (classic)rs1057517774
ClinGenrs1057517774
ebirs1057517774
HLIrs1057517774
Exacrs1057517774
Gnomadrs1057517774
Varsomers1057517774
LitVarrs1057517774
Maprs1057517774
PheGenIrs1057517774
Biobankrs1057517774
1000 genomesrs1057517774
hgdprs1057517774
ensemblrs1057517774
geneviewrs1057517774
scholarrs1057517774
googlers1057517774
pharmgkbrs1057517774
gwascentralrs1057517774
openSNPrs1057517774
23andMers1057517774
23andMe allrs1057517774
SNPshotrs1057517774
SNPdbers1057517774
MSV3drs1057517774
GWAS Ctlgrs1057517774
Max Magnitude0
ClinVar
Risk rs1057517774(G;G)
Alt rs1057517774(G;G)
Reference Rs1057517774(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYO7A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.76873891C>G
CLNSRC
CLNACC RCV000413907.1,