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rs58901407

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs58901407(G;G)
Make rs58901407(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position40822137
GeneKRT10, TMEM99
is asnp
is mentioned by
dbSNPrs58901407
ebirs58901407
HLIrs58901407
Exacrs58901407
Varsomers58901407
Maprs58901407
PheGenIrs58901407
hapmaprs58901407
1000 genomesrs58901407
hgdprs58901407
ensemblrs58901407
gopubmedrs58901407
geneviewrs58901407
scholarrs58901407
googlers58901407
pharmgkbrs58901407
gwascentralrs58901407
openSNPrs58901407
23andMers58901407
23andMe allrs58901407
SNP Nexus

SNPshotrs58901407
SNPdbers58901407
MSV3drs58901407
GWAS Ctlgrs58901407
Max Magnitude0
OMIM148080
Desc
Variant0011
Relatedalso
ClinVar
Risk rs58901407(C,G;C,G)
Alt rs58901407(C,G;C,G)
Reference rs58901407(T;T)
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.38978389A>C; NC_000017.10:g.38978389A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015678.21, RCV000056491.1, RCV000015680.25, RCV000056490.1,