rs1057519328

Orientation

minus

Stabilized

minus

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

Make rs1057519328(C;G)

Make rs1057519328(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

3249592

Gene

MEFV

is a	snp
is	mentioned by
dbSNP	rs1057519328
dbSNP (classic)	rs1057519328
ClinGen	rs1057519328
ebi	rs1057519328
HLI	rs1057519328
Exac	rs1057519328
Gnomad	rs1057519328
Varsome	rs1057519328
LitVar	rs1057519328
Map	rs1057519328
PheGenI	rs1057519328
Biobank	rs1057519328
1000 genomes	rs1057519328
hgdp	rs1057519328
ensembl	rs1057519328
geneview	rs1057519328
scholar	rs1057519328
google	rs1057519328
pharmgkb	rs1057519328
gwascentral	rs1057519328
openSNP	rs1057519328
23andMe	rs1057519328
SNPshot	rs1057519328
SNPdbe	rs1057519328
MSV3d	rs1057519328
GWAS Ctlg	rs1057519328

Max Magnitude

0

ClinVar
Risk	rs1057519328(G;G)
Alt	rs1057519328(G;G)
Reference	Rs1057519328(C;C)
Significance	Pathogenic
Disease	Behcet's syndrome
Variation	info
Gene	MEFV
CLNDBN	Behcet's syndrome
Reversed	1
HGVS	NC_000016.9:g.3299592G>C
CLNSRC
CLNACC	RCV000416346.1,