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rs267607462

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607462(C;C)
Make rs267607462(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position52488365
GeneKRT6A, LOC107984511
is asnp
is mentioned by
dbSNPrs267607462
dbSNP (old)rs267607462
ClinGenrs267607462
ebirs267607462
HLIrs267607462
Exacrs267607462
Gnomadrs267607462
Varsomers267607462
Maprs267607462
PheGenIrs267607462
Biobankrs267607462
1000 genomesrs267607462
hgdprs267607462
ensemblrs267607462
gopubmedrs267607462
geneviewrs267607462
scholarrs267607462
googlers267607462
pharmgkbrs267607462
gwascentralrs267607462
openSNPrs267607462
23andMers267607462
23andMe allrs267607462
SNPshotrs267607462
SNPdbers267607462
MSV3drs267607462
GWAS Ctlgrs267607462
Max Magnitude0
ClinVar
Risk rs267607462(C;C)
Alt rs267607462(C;C)
Reference Rs267607462(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT6A
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.52882149C>G
CLNSRC UniProtKB (protein)
CLNACC RCV000056990.2,