rs770302956

Orientation

plus

Stabilized

plus

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

Make rs770302956(C;T)

Make rs770302956(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

209629732

Gene

LAMB3

is a	snp
is	mentioned by
dbSNP	rs770302956
dbSNP (classic)	rs770302956
ClinGen	rs770302956
ebi	rs770302956
HLI	rs770302956
Exac	rs770302956
Gnomad	rs770302956
Varsome	rs770302956
LitVar	rs770302956
Map	rs770302956
PheGenI	rs770302956
Biobank	rs770302956
1000 genomes	rs770302956
hgdp	rs770302956
ensembl	rs770302956
geneview	rs770302956
scholar	rs770302956
google	rs770302956
pharmgkb	rs770302956
gwascentral	rs770302956
openSNP	rs770302956
23andMe	rs770302956
SNPshot	rs770302956
SNPdbe	rs770302956
MSV3d	rs770302956
GWAS Ctlg	rs770302956

Max Magnitude

0

ClinVar
Risk	rs770302956(T;T)
Alt	rs770302956(T;T)
Reference	Rs770302956(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LAMB3
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.209803077C>T
CLNSRC
CLNACC	RCV000255633.1,