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rs58949162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs58949162(G;T)
Make rs58949162(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position52676316
GeneKRT1
is asnp
is mentioned by
dbSNPrs58949162
dbSNP (classic)rs58949162
ClinGenrs58949162
ebirs58949162
HLIrs58949162
Exacrs58949162
Gnomadrs58949162
Varsomers58949162
LitVarrs58949162
Maprs58949162
PheGenIrs58949162
Biobankrs58949162
1000 genomesrs58949162
hgdprs58949162
ensemblrs58949162
geneviewrs58949162
scholarrs58949162
googlers58949162
pharmgkbrs58949162
gwascentralrs58949162
openSNPrs58949162
23andMers58949162
SNPshotrs58949162
SNPdbers58949162
MSV3drs58949162
GWAS Ctlgrs58949162
Max Magnitude0
ClinVar
Risk rs58949162(C;C) rs58949162(T;T)
Alt rs58949162(C;C) rs58949162(T;T)
Reference Rs58949162(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.53070100C>A; NC_000012.11:g.53070100C>G
CLNSRC
CLNACC RCV000057061.1, RCV000444525.1,