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rs267607473

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607473(A;A)
Make rs267607473(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position52447821
GeneKRT6B
is asnp
is mentioned by
dbSNPrs267607473
dbSNP (old)rs267607473
ClinGenrs267607473
ebirs267607473
HLIrs267607473
Exacrs267607473
Gnomadrs267607473
Varsomers267607473
Maprs267607473
PheGenIrs267607473
Biobankrs267607473
1000 genomesrs267607473
hgdprs267607473
ensemblrs267607473
gopubmedrs267607473
geneviewrs267607473
scholarrs267607473
googlers267607473
pharmgkbrs267607473
gwascentralrs267607473
openSNPrs267607473
23andMers267607473
23andMe allrs267607473
SNPshotrs267607473
SNPdbers267607473
MSV3drs267607473
GWAS Ctlgrs267607473
Max Magnitude0
ClinVar
Risk rs267607473(A;A)
Alt rs267607473(A;A)
Reference Rs267607473(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT6B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.52841605C>T
CLNSRC
CLNACC RCV000057022.2,