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rs1057520647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520647(C;T)
Make rs1057520647(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position30694499
GeneGK
is asnp
is mentioned by
dbSNPrs1057520647
dbSNP (old)rs1057520647
ClinGenrs1057520647
ebirs1057520647
HLIrs1057520647
Exacrs1057520647
Gnomadrs1057520647
Varsomers1057520647
Maprs1057520647
PheGenIrs1057520647
Biobankrs1057520647
1000 genomesrs1057520647
hgdprs1057520647
ensemblrs1057520647
gopubmedrs1057520647
geneviewrs1057520647
scholarrs1057520647
googlers1057520647
pharmgkbrs1057520647
gwascentralrs1057520647
openSNPrs1057520647
23andMers1057520647
23andMe allrs1057520647
SNPshotrs1057520647
SNPdbers1057520647
MSV3drs1057520647
GWAS Ctlgrs1057520647
Max Magnitude0
ClinVar
Risk rs1057520647(T;T)
Alt rs1057520647(T;T)
Reference Rs1057520647(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GK
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.30712616C>T
CLNSRC
CLNACC RCV000433135.1,