rs886040969

Orientation

plus

Stabilized

plus

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

Make rs886040969(A;A)

Make rs886040969(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50712357

Gene

NOD2

is a	snp
is	mentioned by
dbSNP	rs886040969
dbSNP (classic)	rs886040969
ClinGen	rs886040969
ebi	rs886040969
HLI	rs886040969
Exac	rs886040969
Gnomad	rs886040969
Varsome	rs886040969
LitVar	rs886040969
Map	rs886040969
PheGenI	rs886040969
Biobank	rs886040969
1000 genomes	rs886040969
hgdp	rs886040969
ensembl	rs886040969
geneview	rs886040969
scholar	rs886040969
google	rs886040969
pharmgkb	rs886040969
gwascentral	rs886040969
openSNP	rs886040969
23andMe	rs886040969
SNPshot	rs886040969
SNPdbe	rs886040969
MSV3d	rs886040969
GWAS Ctlg	rs886040969

Max Magnitude

0

ClinVar
Risk	rs886040969(A;A)
Alt	rs886040969(A;A)
Reference	Rs886040969(G;G)
Significance	Pathogenic
Disease	Behcet's syndrome
Variation	info
Gene	NOD2
CLNDBN	Behcet's syndrome
Reversed	0
HGVS	NC_000016.9:g.50746268G>A
CLNSRC
CLNACC	RCV000258046.1,