rs758026399

Orientation

plus

Stabilized

plus

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

Make rs758026399(C;T)

Make rs758026399(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

109586765

Gene

MVK

is a	snp
is	mentioned by
dbSNP	rs758026399
dbSNP (classic)	rs758026399
ClinGen	rs758026399
ebi	rs758026399
HLI	rs758026399
Exac	rs758026399
Gnomad	rs758026399
Varsome	rs758026399
LitVar	rs758026399
Map	rs758026399
PheGenI	rs758026399
Biobank	rs758026399
1000 genomes	rs758026399
hgdp	rs758026399
ensembl	rs758026399
geneview	rs758026399
scholar	rs758026399
google	rs758026399
pharmgkb	rs758026399
gwascentral	rs758026399
openSNP	rs758026399
23andMe	rs758026399
SNPshot	rs758026399
SNPdbe	rs758026399
MSV3d	rs758026399
GWAS Ctlg	rs758026399

Max Magnitude

0

ClinVar
Risk	rs758026399(T;T)
Alt	rs758026399(T;T)
Reference	Rs758026399(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MVK
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.110024570C>T
CLNSRC
CLNACC	RCV000221444.1,