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rs267607463

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607463(C;C)
Make rs267607463(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position52488359
GeneKRT6A, LOC107984511
is asnp
is mentioned by
dbSNPrs267607463
dbSNP (old)rs267607463
ClinGenrs267607463
ebirs267607463
HLIrs267607463
Exacrs267607463
Gnomadrs267607463
Varsomers267607463
Maprs267607463
PheGenIrs267607463
Biobankrs267607463
1000 genomesrs267607463
hgdprs267607463
ensemblrs267607463
gopubmedrs267607463
geneviewrs267607463
scholarrs267607463
googlers267607463
pharmgkbrs267607463
gwascentralrs267607463
openSNPrs267607463
23andMers267607463
23andMe allrs267607463
SNPshotrs267607463
SNPdbers267607463
MSV3drs267607463
GWAS Ctlgrs267607463
Max Magnitude0
ClinVar
Risk rs267607463(C;C)
Alt rs267607463(C;C)
Reference Rs267607463(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT6A
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.52882143A>G
CLNSRC UniProtKB (protein)
CLNACC RCV000056992.1,