rs1057516727

Orientation

plus

Stabilized

plus

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

Make rs1057516727(-;-)

Make rs1057516727(-;CA)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

183236544

Gene

LAMC2

is a	snp
is	mentioned by
dbSNP	rs1057516727
dbSNP (classic)	rs1057516727
ClinGen	rs1057516727
ebi	rs1057516727
HLI	rs1057516727
Exac	rs1057516727
Gnomad	rs1057516727
Varsome	rs1057516727
LitVar	rs1057516727
Map	rs1057516727
PheGenI	rs1057516727
Biobank	rs1057516727
1000 genomes	rs1057516727
hgdp	rs1057516727
ensembl	rs1057516727
geneview	rs1057516727
scholar	rs1057516727
google	rs1057516727
pharmgkb	rs1057516727
gwascentral	rs1057516727
openSNP	rs1057516727
23andMe	rs1057516727
SNPshot	rs1057516727
SNPdbe	rs1057516727
MSV3d	rs1057516727
GWAS Ctlg	rs1057516727

Max Magnitude

0

ClinVar
Risk	rs1057516727(-;-)
Alt	rs1057516727(-;-)
Reference	Rs1057516727(CA;CA)
Significance	Probable-Pathogenic
Disease	Junctional epidermolysis bullosa gravis of Herlitz
Variation	info
Gene	LAMC2
CLNDBN	Junctional epidermolysis bullosa gravis of Herlitz
Reversed	0
HGVS	NC_000001.10:g.183205679_183205680delCA
CLNSRC
CLNACC	RCV000410843.1,