rs774133746

Orientation

plus

Stabilized

plus

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

Make rs774133746(C;T)

Make rs774133746(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

23928148

Gene

LAMA3

is a	snp
is	mentioned by
dbSNP	rs774133746
dbSNP (classic)	rs774133746
ClinGen	rs774133746
ebi	rs774133746
HLI	rs774133746
Exac	rs774133746
Gnomad	rs774133746
Varsome	rs774133746
LitVar	rs774133746
Map	rs774133746
PheGenI	rs774133746
Biobank	rs774133746
1000 genomes	rs774133746
hgdp	rs774133746
ensembl	rs774133746
geneview	rs774133746
scholar	rs774133746
google	rs774133746
pharmgkb	rs774133746
gwascentral	rs774133746
openSNP	rs774133746
23andMe	rs774133746
SNPshot	rs774133746
SNPdbe	rs774133746
MSV3d	rs774133746
GWAS Ctlg	rs774133746

Max Magnitude

0

ClinVar
Risk	rs774133746(T;T)
Alt	rs774133746(T;T)
Reference	Rs774133746(C;C)
Significance	Probable-Pathogenic
Disease	Junctional epidermolysis bullosa gravis of Herlitz
Variation	info
Gene	LAMA3
CLNDBN	Junctional epidermolysis bullosa gravis of Herlitz
Reversed	0
HGVS	NC_000018.9:g.21508112C>T
CLNSRC
CLNACC	RCV000411334.1,