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rs1057520781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520781(C;C)
Make rs1057520781(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position30668120
GeneGK
is asnp
is mentioned by
dbSNPrs1057520781
dbSNP (old)rs1057520781
ClinGenrs1057520781
ebirs1057520781
HLIrs1057520781
Exacrs1057520781
Gnomadrs1057520781
Varsomers1057520781
Maprs1057520781
PheGenIrs1057520781
Biobankrs1057520781
1000 genomesrs1057520781
hgdprs1057520781
ensemblrs1057520781
gopubmedrs1057520781
geneviewrs1057520781
scholarrs1057520781
googlers1057520781
pharmgkbrs1057520781
gwascentralrs1057520781
openSNPrs1057520781
23andMers1057520781
23andMe allrs1057520781
SNPshotrs1057520781
SNPdbers1057520781
MSV3drs1057520781
GWAS Ctlgrs1057520781
Max Magnitude0
ClinVar
Risk rs1057520781(C;C)
Alt rs1057520781(C;C)
Reference Rs1057520781(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GK
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.30686237T>C
CLNSRC
CLNACC RCV000440001.1,