rs58918655

Orientation

minus

Stabilized

minus

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

Make rs58918655(G;G)

Make rs58918655(G;T)

Reference

GRCh37 37.1/132

Chromosome

17

Position

40866768

Gene	KRT12, LOC105371777

is a	snp
is	mentioned by
dbSNP	rs58918655
dbSNP (classic)	rs58918655
ClinGen	rs58918655
ebi	rs58918655
HLI	rs58918655
Exac	rs58918655
Gnomad	rs58918655
Varsome	rs58918655
LitVar	rs58918655
Map	rs58918655
PheGenI	rs58918655
Biobank	rs58918655
1000 genomes	rs58918655
hgdp	rs58918655
ensembl	rs58918655
geneview	rs58918655
scholar	rs58918655
google	rs58918655
pharmgkb	rs58918655
gwascentral	rs58918655
openSNP	rs58918655
23andMe	rs58918655
SNPshot	rs58918655
SNPdbe	rs58918655
MSV3d	rs58918655
GWAS Ctlg	rs58918655

Max Magnitude

0

OMIM	601687
Desc
Variant	0006
Related	also

ClinVar
Risk	rs58918655(G;G)
Alt	rs58918655(G;G)
Reference	Rs58918655(T;T)
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.39023020A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008388.5, RCV000056425.1,