rs59897026

Orientation

minus

Stabilized

minus

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

Make rs59897026(C;C)

Make rs59897026(C;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

41505219

Gene

KRT13

is a	snp
is	mentioned by
dbSNP	rs59897026
dbSNP (classic)	rs59897026
ClinGen	rs59897026
ebi	rs59897026
HLI	rs59897026
Exac	rs59897026
Gnomad	rs59897026
Varsome	rs59897026
LitVar	rs59897026
Map	rs59897026
PheGenI	rs59897026
Biobank	rs59897026
1000 genomes	rs59897026
hgdp	rs59897026
ensembl	rs59897026
geneview	rs59897026
scholar	rs59897026
google	rs59897026
pharmgkb	rs59897026
gwascentral	rs59897026
openSNP	rs59897026
23andMe	rs59897026
SNPshot	rs59897026
SNPdbe	rs59897026
MSV3d	rs59897026
GWAS Ctlg	rs59897026

Max Magnitude

0

ClinVar
Risk	rs59897026(C;C)
Alt	rs59897026(C;C)
Reference	Rs59897026(T;T)
Significance	Pathogenic
Disease	not provided White sponge nevus 2
Variation	info
Gene	KRT13
CLNDBN	not provided White sponge nevus 2
Reversed	1
HGVS	NC_000017.10:g.39661471A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000057206.1, RCV000116204.2,