rs746055479

Orientation

plus

Stabilized

plus

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

Make rs746055479(A;A)

Make rs746055479(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

50712108

Gene

NOD2

is a	snp
is	mentioned by
dbSNP	rs746055479
dbSNP (classic)	rs746055479
ClinGen	rs746055479
ebi	rs746055479
HLI	rs746055479
Exac	rs746055479
Gnomad	rs746055479
Varsome	rs746055479
LitVar	rs746055479
Map	rs746055479
PheGenI	rs746055479
Biobank	rs746055479
1000 genomes	rs746055479
hgdp	rs746055479
ensembl	rs746055479
geneview	rs746055479
scholar	rs746055479
google	rs746055479
pharmgkb	rs746055479
gwascentral	rs746055479
openSNP	rs746055479
23andMe	rs746055479
SNPshot	rs746055479
SNPdbe	rs746055479
MSV3d	rs746055479
GWAS Ctlg	rs746055479

Max Magnitude

0

ClinVar
Risk	rs746055479(A;A) rs746055479(T;T)
Alt	rs746055479(A;A) rs746055479(T;T)
Reference	Rs746055479(G;G)
Significance	Pathogenic
Disease	Behcet's syndrome
Variation	info
Gene	NOD2
CLNDBN	Behcet's syndrome
Reversed	0
HGVS	NC_000016.9:g.50746019G>T
CLNSRC
CLNACC	RCV000258056.1,