rs755659290

Orientation

plus

Stabilized

plus

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

Make rs755659290(C;C)

Make rs755659290(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

3249480

Gene

MEFV

is a	snp
is	mentioned by
dbSNP	rs755659290
dbSNP (classic)	rs755659290
ClinGen	rs755659290
ebi	rs755659290
HLI	rs755659290
Exac	rs755659290
Gnomad	rs755659290
Varsome	rs755659290
LitVar	rs755659290
Map	rs755659290
PheGenI	rs755659290
Biobank	rs755659290
1000 genomes	rs755659290
hgdp	rs755659290
ensembl	rs755659290
geneview	rs755659290
scholar	rs755659290
google	rs755659290
pharmgkb	rs755659290
gwascentral	rs755659290
openSNP	rs755659290
23andMe	rs755659290
SNPshot	rs755659290
SNPdbe	rs755659290
MSV3d	rs755659290
GWAS Ctlg	rs755659290

Max Magnitude

0

ClinVar
Risk	rs755659290(C;C)
Alt	rs755659290(C;C)
Reference	Rs755659290(T;T)
Significance	Pathogenic
Disease	Behcet's syndrome
Variation	info
Gene	MEFV
CLNDBN	Behcet's syndrome
Reversed	0
HGVS	NC_000016.9:g.3299480T>C
CLNSRC
CLNACC	RCV000416328.1,