rs151190720

Orientation

plus

Stabilized

plus

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

Make rs151190720(C;T)

Make rs151190720(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

183236593

Gene

LAMC2

is a	snp
is	mentioned by
dbSNP	rs151190720
dbSNP (classic)	rs151190720
ClinGen	rs151190720
ebi	rs151190720
HLI	rs151190720
Exac	rs151190720
Gnomad	rs151190720
Varsome	rs151190720
LitVar	rs151190720
Map	rs151190720
PheGenI	rs151190720
Biobank	rs151190720
1000 genomes	rs151190720
hgdp	rs151190720
ensembl	rs151190720
geneview	rs151190720
scholar	rs151190720
google	rs151190720
pharmgkb	rs151190720
gwascentral	rs151190720
openSNP	rs151190720
23andMe	rs151190720
SNPshot	rs151190720
SNPdbe	rs151190720
MSV3d	rs151190720
GWAS Ctlg	rs151190720

Max Magnitude

0

ClinVar
Risk	rs151190720(G;G) rs151190720(T;T)
Alt	rs151190720(G;G) rs151190720(T;T)
Reference	Rs151190720(C;C)
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.183205728C>T
CLNSRC
CLNACC	RCV000411449.1,