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rs886039403

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039403(A;A)
Make rs886039403(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position52519741
GeneKRT5
is asnp
is mentioned by
dbSNPrs886039403
dbSNP (classic)rs886039403
ClinGenrs886039403
ebirs886039403
HLIrs886039403
Exacrs886039403
Gnomadrs886039403
Varsomers886039403
LitVarrs886039403
Maprs886039403
PheGenIrs886039403
Biobankrs886039403
1000 genomesrs886039403
hgdprs886039403
ensemblrs886039403
geneviewrs886039403
scholarrs886039403
googlers886039403
pharmgkbrs886039403
gwascentralrs886039403
openSNPrs886039403
23andMers886039403
23andMe allrs886039403
SNPshotrs886039403
SNPdbers886039403
MSV3drs886039403
GWAS Ctlgrs886039403
Max Magnitude0
ClinVar
Risk rs886039403(A;A)
Alt rs886039403(A;A)
Reference Rs886039403(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.52913525C>T
CLNSRC
CLNACC RCV000255331.1,