rs786201004

Orientation

minus

Stabilized

minus

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

Make rs786201004(-;G)

Make rs786201004(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

209615395

Gene

LAMB3

is a	snp
is	mentioned by
dbSNP	rs786201004
dbSNP (classic)	rs786201004
ClinGen	rs786201004
ebi	rs786201004
HLI	rs786201004
Exac	rs786201004
Gnomad	rs786201004
Varsome	rs786201004
LitVar	rs786201004
Map	rs786201004
PheGenI	rs786201004
Biobank	rs786201004
1000 genomes	rs786201004
hgdp	rs786201004
ensembl	rs786201004
geneview	rs786201004
scholar	rs786201004
google	rs786201004
pharmgkb	rs786201004
gwascentral	rs786201004
openSNP	rs786201004
23andMe	rs786201004
SNPshot	rs786201004
SNPdbe	rs786201004
MSV3d	rs786201004
GWAS Ctlg	rs786201004

Max Magnitude

0

ClinVar
Risk	rs786201004(G;G)
Alt	rs786201004(G;G)
Reference	Rs786201004(-;-)
Significance	Pathogenic
Disease	Amelogenesis imperfecta
Variation	info
Gene	LAMB3
CLNDBN	Amelogenesis imperfecta, type IA
Reversed	1
HGVS	NC_000001.10:g.209788741dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000157637.4,