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rs59856285

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs59856285(C;T)
Make rs59856285(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position41612310
GeneKRT16
is asnp
is mentioned by
dbSNPrs59856285
ebirs59856285
HLIrs59856285
Exacrs59856285
Varsomers59856285
Maprs59856285
PheGenIrs59856285
hapmaprs59856285
1000 genomesrs59856285
hgdprs59856285
ensemblrs59856285
gopubmedrs59856285
geneviewrs59856285
scholarrs59856285
googlers59856285
pharmgkbrs59856285
gwascentralrs59856285
openSNPrs59856285
23andMers59856285
23andMe allrs59856285
SNP Nexus

SNPshotrs59856285
SNPdbers59856285
MSV3drs59856285
GWAS Ctlgrs59856285
Max Magnitude0
OMIM148067
Desc
Variant0002
Relatedalso


ClinVar
Risk rs59856285(T;T)
Alt rs59856285(T;T)
Reference rs59856285(C;C)
Significance Pathogenic
Disease Palmoplantar keratoderma not provided
Variation info
Gene KRT16
CLNDBN Palmoplantar keratoderma, nonepidermolytic, focal not provided
Reversed 1
HGVS NC_000017.10:g.39768562G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015705.27, RCV000057038.1,