rs587776845

Orientation

plus

Stabilized

minus

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

Make rs587776845(-;TTG)

Make rs587776845(TTG;TTG)

Reference

GRCh38 38.1/142

Chromosome

12

Position

52813639

Gene

KRT4

is a	snp
is	mentioned by
dbSNP	rs587776845
dbSNP (classic)	rs587776845
ClinGen	rs587776845
ebi	rs587776845
HLI	rs587776845
Exac	rs587776845
Gnomad	rs587776845
Varsome	rs587776845
LitVar	rs587776845
Map	rs587776845
PheGenI	rs587776845
Biobank	rs587776845
1000 genomes	rs587776845
hgdp	rs587776845
ensembl	rs587776845
geneview	rs587776845
scholar	rs587776845
google	rs587776845
pharmgkb	rs587776845
gwascentral	rs587776845
openSNP	rs587776845
23andMe	rs587776845
SNPshot	rs587776845
SNPdbe	rs587776845
MSV3d	rs587776845
GWAS Ctlg	rs587776845

Max Magnitude

0

ClinVar
Risk	rs587776845(TTG;TTG)
Alt	rs587776845(TTG;TTG)
Reference	Rs587776845(-;-)
Significance	Pathogenic
Disease	White sponge nevus of cannon
Variation	info
Gene	KRT4
CLNDBN	White sponge nevus of cannon
Reversed	1
HGVS	NC_000012.11:g.53207423_53207424insTTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018421.28,