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rs587776816

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776816(C;T)
Make rs587776816(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position40819516
GeneKRT10, TMEM99
is asnp
is mentioned by
dbSNPrs587776816
ebirs587776816
HLIrs587776816
Exacrs587776816
Varsomers587776816
Maprs587776816
PheGenIrs587776816
hapmaprs587776816
1000 genomesrs587776816
hgdprs587776816
ensemblrs587776816
gopubmedrs587776816
geneviewrs587776816
scholarrs587776816
googlers587776816
pharmgkbrs587776816
gwascentralrs587776816
openSNPrs587776816
23andMers587776816
23andMe allrs587776816
SNP Nexus

SNPshotrs587776816
SNPdbers587776816
MSV3drs587776816
GWAS Ctlgrs587776816
Max Magnitude0
ClinVar
Risk rs587776816(C,T;C,T)
Alt rs587776816(C,T;C,T)
Reference rs587776816(G;G)
Significance Pathogenic
Disease Erythroderma
Variation info
Gene KRT10 TMEM99
CLNDBN Erythroderma, ichthyosiform, congenital reticular
Reversed 1
HGVS NC_000017.10:g.38975768C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015683.27,