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rs58181827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCT;CCT) 0 common in clinvar
(D;D) 0
Make rs58181827(-;-)
Make rs58181827(-;CCT)
ReferenceGRCh38 38.1/142
Chromosome17
Position41612298
GeneKRT16
is asnp
is mentioned by
dbSNPrs58181827
ebirs58181827
HLIrs58181827
Exacrs58181827
Varsomers58181827
Maprs58181827
PheGenIrs58181827
hapmaprs58181827
1000 genomesrs58181827
hgdprs58181827
ensemblrs58181827
gopubmedrs58181827
geneviewrs58181827
scholarrs58181827
googlers58181827
pharmgkbrs58181827
gwascentralrs58181827
openSNPrs58181827
23andMers58181827
23andMe allrs58181827
SNP Nexus

SNPshotrs58181827
SNPdbers58181827
MSV3drs58181827
GWAS Ctlgrs58181827
Max Magnitude0


ClinVar
Risk rs58181827(;)
Alt rs58181827(;)
Reference rs58181827(CCT;CCT)
Significance Pathogenic
Disease Pachyonychia congenita not provided
Variation info
Gene KRT16
CLNDBN Pachyonychia congenita, type 1 not provided
Reversed 1
HGVS NC_000017.10:g.39768550_39768552delAGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000015707.27, RCV000057041.1,