rs60035576

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs60035576(C;T)

Make rs60035576(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

40819590

Gene	KRT10, TMEM99

is a	snp
is	mentioned by
dbSNP	rs60035576
dbSNP (classic)	rs60035576
ClinGen	rs60035576
ebi	rs60035576
HLI	rs60035576
Exac	rs60035576
Gnomad	rs60035576
Varsome	rs60035576
LitVar	rs60035576
Map	rs60035576
PheGenI	rs60035576
Biobank	rs60035576
1000 genomes	rs60035576
hgdp	rs60035576
ensembl	rs60035576
geneview	rs60035576
scholar	rs60035576
google	rs60035576
pharmgkb	rs60035576
gwascentral	rs60035576
openSNP	rs60035576
23andMe	rs60035576
SNPshot	rs60035576
SNPdbe	rs60035576
MSV3d	rs60035576
GWAS Ctlg	rs60035576

Max Magnitude

0

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,