rs104895311

Orientation

plus

Stabilized

plus

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

Make rs104895311(A;A)

Make rs104895311(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

109586058

Gene

MVK

is a	snp
is	mentioned by
dbSNP	rs104895311
dbSNP (classic)	rs104895311
ClinGen	rs104895311
ebi	rs104895311
HLI	rs104895311
Exac	rs104895311
Gnomad	rs104895311
Varsome	rs104895311
LitVar	rs104895311
Map	rs104895311
PheGenI	rs104895311
Biobank	rs104895311
1000 genomes	rs104895311
hgdp	rs104895311
ensembl	rs104895311
geneview	rs104895311
scholar	rs104895311
google	rs104895311
pharmgkb	rs104895311
gwascentral	rs104895311
openSNP	rs104895311
23andMe	rs104895311
SNPshot	rs104895311
SNPdbe	rs104895311
MSV3d	rs104895311
GWAS Ctlg	rs104895311

Max Magnitude

0

ClinVar
Risk	rs104895311(A;A)
Alt	rs104895311(A;A)
Reference	Rs104895311(G;G)
Significance	Pathogenic
Disease	Hyperimmunoglobulin D with periodic fever
Variation	info
Gene	MVK
CLNDBN	Hyperimmunoglobulin D with periodic fever
Reversed	0
HGVS	NC_000012.11:g.110023863G>A
CLNSRC
CLNACC	RCV000083849.2,