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rs267607384

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs267607384(-;-)
Make rs267607384(-;CG)
ReferenceGRCh38 38.1/142
Chromosome17
Position40818974
GeneKRT10, TMEM99
is asnp
is mentioned by
dbSNPrs267607384
ebirs267607384
HLIrs267607384
Exacrs267607384
Varsomers267607384
Maprs267607384
PheGenIrs267607384
hapmaprs267607384
1000 genomesrs267607384
hgdprs267607384
ensemblrs267607384
gopubmedrs267607384
geneviewrs267607384
scholarrs267607384
googlers267607384
pharmgkbrs267607384
gwascentralrs267607384
openSNPrs267607384
23andMers267607384
23andMe allrs267607384
SNP Nexus

SNPshotrs267607384
SNPdbers267607384
MSV3drs267607384
GWAS Ctlgrs267607384
Max Magnitude0
ClinVar
Risk rs267607384(;)
Alt rs267607384(;)
Reference rs267607384(CG;CG)
Significance Pathogenic
Disease Erythroderma not provided
Variation info
Gene KRT10 TMEM99
CLNDBN Erythroderma, ichthyosiform, congenital reticular not provided
Reversed 1
HGVS NC_000017.10:g.38975226_38975227delCG
CLNSRC OMIM Allelic Variant
CLNACC RCV000015685.26, RCV000056488.1,