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rs587776817

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776817(-;-)
Make rs587776817(-;G)
Make rs587776817(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position40819086
GeneKRT10, TMEM99
is asnp
is mentioned by
dbSNPrs587776817
ebirs587776817
HLIrs587776817
Exacrs587776817
Varsomers587776817
Maprs587776817
PheGenIrs587776817
hapmaprs587776817
1000 genomesrs587776817
hgdprs587776817
ensemblrs587776817
gopubmedrs587776817
geneviewrs587776817
scholarrs587776817
googlers587776817
pharmgkbrs587776817
gwascentralrs587776817
openSNPrs587776817
23andMers587776817
23andMe allrs587776817
SNP Nexus

SNPshotrs587776817
SNPdbers587776817
MSV3drs587776817
GWAS Ctlgrs587776817
Max Magnitude0
ClinVar
Risk rs587776817(G;G)
Alt rs587776817(G;G)
Reference rs587776817(;)
Significance Pathogenic
Disease Erythroderma
Variation info
Gene KRT10 TMEM99
CLNDBN Erythroderma, ichthyosiform, congenital reticular
Reversed 0
HGVS NC_000017.10:g.38975338dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000015684.26,