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rs267607448

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607448(C;T)
Make rs267607448(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position52516665
GeneKRT5
is asnp
is mentioned by
dbSNPrs267607448
dbSNP (classic)rs267607448
ClinGenrs267607448
ebirs267607448
HLIrs267607448
Exacrs267607448
Gnomadrs267607448
Varsomers267607448
LitVarrs267607448
Maprs267607448
PheGenIrs267607448
Biobankrs267607448
1000 genomesrs267607448
hgdprs267607448
ensemblrs267607448
geneviewrs267607448
scholarrs267607448
googlers267607448
pharmgkbrs267607448
gwascentralrs267607448
openSNPrs267607448
23andMers267607448
23andMe allrs267607448
SNPshotrs267607448
SNPdbers267607448
MSV3drs267607448
GWAS Ctlgrs267607448
Max Magnitude0
ClinVar
Risk rs267607448(T;T)
Alt rs267607448(T;T)
Reference Rs267607448(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.52910449G>A
CLNSRC
CLNACC RCV000056559.2,