rs58410481

Orientation

minus

Stabilized

minus

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

Make rs58410481(A;G)

Make rs58410481(G;G)

Reference

GRCh37 37.1/132

Chromosome

17

Position

39023036

Gene

KRT12

is a	snp
is	mentioned by
dbSNP	rs58410481
dbSNP (classic)	rs58410481
ClinGen	rs58410481
ebi	rs58410481
HLI	rs58410481
Exac	rs58410481
Gnomad	rs58410481
Varsome	rs58410481
LitVar	rs58410481
Map	rs58410481
PheGenI	rs58410481
Biobank	rs58410481
1000 genomes	rs58410481
hgdp	rs58410481
ensembl	rs58410481
geneview	rs58410481
scholar	rs58410481
google	rs58410481
pharmgkb	rs58410481
gwascentral	rs58410481
openSNP	rs58410481
23andMe	rs58410481
SNPshot	rs58410481
SNPdbe	rs58410481
MSV3d	rs58410481
GWAS Ctlg	rs58410481

Max Magnitude

0

OMIM	601687
Desc
Variant	0003
Related	also

ClinVar
Risk	rs58410481(G;G)
Alt	rs58410481(G;G)
Reference	Rs58410481(A;A)
Significance	Pathogenic
Disease	Meesman's corneal dystrophy not provided
Variation	info
Gene	KRT12
CLNDBN	Meesman's corneal dystrophy not provided
Reversed	1
HGVS	NC_000017.10:g.39023036T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008385.4, RCV000056420.1,