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rs58645163

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs58645163(A;A)
Make rs58645163(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position41583346
GeneKRT14
is asnp
is mentioned by
dbSNPrs58645163
dbSNP (old)rs58645163
ClinGenrs58645163
ebirs58645163
HLIrs58645163
Exacrs58645163
Gnomadrs58645163
Varsomers58645163
Maprs58645163
PheGenIrs58645163
Biobankrs58645163
1000 genomesrs58645163
hgdprs58645163
ensemblrs58645163
gopubmedrs58645163
geneviewrs58645163
scholarrs58645163
googlers58645163
pharmgkbrs58645163
gwascentralrs58645163
openSNPrs58645163
23andMers58645163
23andMe allrs58645163
SNPshotrs58645163
SNPdbers58645163
MSV3drs58645163
GWAS Ctlgrs58645163
Max Magnitude0
ClinVar
Risk rs58645163(A;A) rs58645163(C;C)
Alt rs58645163(A;A) rs58645163(C;C)
Reference Rs58645163(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT14
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.39739598C>G; NC_000017.10:g.39739598C>T
CLNSRC
CLNACC RCV000056670.1, RCV000487370.1,