rs786205562

Orientation

minus

Stabilized

minus

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

Make rs786205562(G;T)

Make rs786205562(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

49121728

Gene	LAMB2, USP19

is a	snp
is	mentioned by
dbSNP	rs786205562
dbSNP (classic)	rs786205562
ClinGen	rs786205562
ebi	rs786205562
HLI	rs786205562
Exac	rs786205562
Gnomad	rs786205562
Varsome	rs786205562
LitVar	rs786205562
Map	rs786205562
PheGenI	rs786205562
Biobank	rs786205562
1000 genomes	rs786205562
hgdp	rs786205562
ensembl	rs786205562
geneview	rs786205562
scholar	rs786205562
google	rs786205562
pharmgkb	rs786205562
gwascentral	rs786205562
openSNP	rs786205562
23andMe	rs786205562
SNPshot	rs786205562
SNPdbe	rs786205562
MSV3d	rs786205562
GWAS Ctlg	rs786205562

Max Magnitude

0

ClinVar
Risk	rs786205562(T;T)
Alt	rs786205562(T;T)
Reference	Rs786205562(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LAMB2 USP19
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.49159161C>A
CLNSRC
CLNACC	RCV000171362.1,