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rs60035576

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs60035576(C;T)
Make rs60035576(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position40819590
GeneKRT10, TMEM99
is asnp
is mentioned by
dbSNPrs60035576
ebirs60035576
HLIrs60035576
Exacrs60035576
Varsomers60035576
Maprs60035576
PheGenIrs60035576
hapmaprs60035576
1000 genomesrs60035576
hgdprs60035576
ensemblrs60035576
gopubmedrs60035576
geneviewrs60035576
scholarrs60035576
googlers60035576
pharmgkbrs60035576
gwascentralrs60035576
openSNPrs60035576
23andMers60035576
23andMe allrs60035576
SNP Nexus

SNPshotrs60035576
SNPdbers60035576
MSV3drs60035576
GWAS Ctlgrs60035576
Max Magnitude0
ClinVar
Risk rs60035576(T;T)
Alt rs60035576(T;T)
Reference rs60035576(C;C)
Significance Pathogenic
Disease Bullous ichthyosiform erythroderma not provided
Variation info
Gene KRT10 TMEM99
CLNDBN Bullous ichthyosiform erythroderma not provided
Reversed 1
HGVS NC_000017.10:g.38975842G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022630.25, RCV000056476.1,