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rs1057517928

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517928(C;T)
Make rs1057517928(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position69382591
GeneHK1
is asnp
is mentioned by
dbSNPrs1057517928
dbSNP (old)rs1057517928
ClinGenrs1057517928
ebirs1057517928
HLIrs1057517928
Exacrs1057517928
Gnomadrs1057517928
Varsomers1057517928
Maprs1057517928
PheGenIrs1057517928
Biobankrs1057517928
1000 genomesrs1057517928
hgdprs1057517928
ensemblrs1057517928
gopubmedrs1057517928
geneviewrs1057517928
scholarrs1057517928
googlers1057517928
pharmgkbrs1057517928
gwascentralrs1057517928
openSNPrs1057517928
23andMers1057517928
23andMe allrs1057517928
SNPshotrs1057517928
SNPdbers1057517928
MSV3drs1057517928
GWAS Ctlgrs1057517928
Max Magnitude0
ClinVar
Risk rs1057517928(T;T)
Alt rs1057517928(T;T)
Reference Rs1057517928(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HK1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.71142347C>T
CLNSRC
CLNACC RCV000413860.1,