rs797044882

Orientation

minus

Stabilized

minus

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

Make rs797044882(C;C)

Make rs797044882(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

47848537

Gene

SMAD2

is a	snp
is	mentioned by
dbSNP	rs797044882
dbSNP (classic)	rs797044882
ClinGen	rs797044882
ebi	rs797044882
HLI	rs797044882
Exac	rs797044882
Gnomad	rs797044882
Varsome	rs797044882
LitVar	rs797044882
Map	rs797044882
PheGenI	rs797044882
Biobank	rs797044882
1000 genomes	rs797044882
hgdp	rs797044882
ensembl	rs797044882
geneview	rs797044882
scholar	rs797044882
google	rs797044882
pharmgkb	rs797044882
gwascentral	rs797044882
openSNP	rs797044882
23andMe	rs797044882
SNPshot	rs797044882
SNPdbe	rs797044882
MSV3d	rs797044882
GWAS Ctlg	rs797044882

Max Magnitude

0

ClinVar
Risk	rs797044882(C;C)
Alt	rs797044882(C;C)
Reference	Rs797044882(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	SMAD2
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000018.9:g.45374908C>G
CLNSRC
CLNACC	RCV000190697.1,