rs59429455

Orientation

minus

Stabilized

minus

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

Make rs59429455(A;A)

Make rs59429455(A;C)

Reference

GRCh38 38.1/141

Chromosome

12

Position

52679785

Gene

KRT1

is a	snp
is	mentioned by
dbSNP	rs59429455
dbSNP (classic)	rs59429455
ClinGen	rs59429455
ebi	rs59429455
HLI	rs59429455
Exac	rs59429455
Gnomad	rs59429455
Varsome	rs59429455
LitVar	rs59429455
Map	rs59429455
PheGenI	rs59429455
Biobank	rs59429455
1000 genomes	rs59429455
hgdp	rs59429455
ensembl	rs59429455
geneview	rs59429455
scholar	rs59429455
google	rs59429455
pharmgkb	rs59429455
gwascentral	rs59429455
openSNP	rs59429455
23andMe	rs59429455
SNPshot	rs59429455
SNPdbe	rs59429455
MSV3d	rs59429455
GWAS Ctlg	rs59429455

Max Magnitude

0

OMIM	139350
Desc
Variant	0008
Related	also

ClinVar
Risk	rs59429455(A;A)
Alt	rs59429455(A;A)
Reference	Rs59429455(C;C)
Significance	Pathogenic
Disease	Bullous ichthyosiform erythroderma not provided
Variation	info
Gene	KRT1
CLNDBN	Bullous ichthyosiform erythroderma not provided
Reversed	1
HGVS	NC_000012.11:g.53073569G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017265.27, RCV000057092.1,