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rs267607400

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607400(C;T)
Make rs267607400(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position41583281
GeneKRT14
is asnp
is mentioned by
dbSNPrs267607400
dbSNP (old)rs267607400
ClinGenrs267607400
ebirs267607400
HLIrs267607400
Exacrs267607400
Gnomadrs267607400
Varsomers267607400
Maprs267607400
PheGenIrs267607400
Biobankrs267607400
1000 genomesrs267607400
hgdprs267607400
ensemblrs267607400
gopubmedrs267607400
geneviewrs267607400
scholarrs267607400
googlers267607400
pharmgkbrs267607400
gwascentralrs267607400
openSNPrs267607400
23andMers267607400
23andMe allrs267607400
SNP Nexus

SNPshotrs267607400
SNPdbers267607400
MSV3drs267607400
GWAS Ctlgrs267607400
Max Magnitude0
ClinVar
Risk rs267607400(T;T)
Alt rs267607400(T;T)
Reference Rs267607400(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT14
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.39739533G>A
CLNSRC
CLNACC RCV000056676.2,