rs104895089

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;C)	3	Carrier of a familial mediterranean fever mutation

Make rs104895089(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

3243449

Gene

MEFV

is a	snp
is	mentioned by
dbSNP	rs104895089
dbSNP (classic)	rs104895089
ClinGen	rs104895089
ebi	rs104895089
HLI	rs104895089
Exac	rs104895089
Gnomad	rs104895089
Varsome	rs104895089
LitVar	rs104895089
Map	rs104895089
PheGenI	rs104895089
Biobank	rs104895089
1000 genomes	rs104895089
hgdp	rs104895089
ensembl	rs104895089
geneview	rs104895089
scholar	rs104895089
google	rs104895089
pharmgkb	rs104895089
gwascentral	rs104895089
openSNP	rs104895089
23andMe	rs104895089
SNPshot	rs104895089
SNPdbe	rs104895089
MSV3d	rs104895089
GWAS Ctlg	rs104895089

Max Magnitude

3

ClinVar
Risk	rs104895089(C;C) rs104895089(G;G)
Alt	rs104895089(C;C) rs104895089(G;G)
Reference	Rs104895089(A;A)
Significance	Untested
Disease	Familial Mediterranean fever
Variation	info
Gene	MEFV
CLNDBN	Familial Mediterranean fever
Reversed	1
HGVS	NC_000016.9:g.3293449T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083732.1,