rs752615209

Orientation

plus

Stabilized

plus

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

Make rs752615209(C;G)

Make rs752615209(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50710956

Gene

NOD2

is a	snp
is	mentioned by
dbSNP	rs752615209
dbSNP (classic)	rs752615209
ClinGen	rs752615209
ebi	rs752615209
HLI	rs752615209
Exac	rs752615209
Gnomad	rs752615209
Varsome	rs752615209
LitVar	rs752615209
Map	rs752615209
PheGenI	rs752615209
Biobank	rs752615209
1000 genomes	rs752615209
hgdp	rs752615209
ensembl	rs752615209
geneview	rs752615209
scholar	rs752615209
google	rs752615209
pharmgkb	rs752615209
gwascentral	rs752615209
openSNP	rs752615209
23andMe	rs752615209
SNPshot	rs752615209
SNPdbe	rs752615209
MSV3d	rs752615209
GWAS Ctlg	rs752615209

Max Magnitude

0

ClinVar
Risk	rs752615209(G;G) rs752615209(T;T)
Alt	rs752615209(G;G) rs752615209(T;T)
Reference	Rs752615209(C;C)
Significance	Pathogenic
Disease	Behcet's syndrome
Variation	info
Gene	NOD2
CLNDBN	Behcet's syndrome
Reversed	0
HGVS	NC_000016.9:g.50744867C>T
CLNSRC
CLNACC	RCV000258859.1,