rs34936594

Orientation

plus

Stabilized

plus

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

Make rs34936594(C;G)

Make rs34936594(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50699655

Gene

NOD2

is a	snp
is	mentioned by
dbSNP	rs34936594
dbSNP (classic)	rs34936594
ClinGen	rs34936594
ebi	rs34936594
HLI	rs34936594
Exac	rs34936594
Gnomad	rs34936594
Varsome	rs34936594
LitVar	rs34936594
Map	rs34936594
PheGenI	rs34936594
Biobank	rs34936594
1000 genomes	rs34936594
hgdp	rs34936594
ensembl	rs34936594
geneview	rs34936594
scholar	rs34936594
google	rs34936594
pharmgkb	rs34936594
gwascentral	rs34936594
openSNP	rs34936594
23andMe	rs34936594
SNPshot	rs34936594
SNPdbe	rs34936594
MSV3d	rs34936594
GWAS Ctlg	rs34936594

Max Magnitude

0

ClinVar
Risk	rs34936594(G;G)
Alt	rs34936594(G;G)
Reference	Rs34936594(C;C)
Significance	Pathogenic
Disease	Behcet's syndrome
Variation	info
Gene	NOD2
CLNDBN	Behcet's syndrome
Reversed	0
HGVS	NC_000016.9:g.50733566C>G
CLNSRC
CLNACC	RCV000258045.1,