rs759997079

Orientation

plus

Stabilized

plus

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

Make rs759997079(A;G)

Make rs759997079(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

109591274

Gene

MVK

is a	snp
is	mentioned by
dbSNP	rs759997079
dbSNP (classic)	rs759997079
ClinGen	rs759997079
ebi	rs759997079
HLI	rs759997079
Exac	rs759997079
Gnomad	rs759997079
Varsome	rs759997079
LitVar	rs759997079
Map	rs759997079
PheGenI	rs759997079
Biobank	rs759997079
1000 genomes	rs759997079
hgdp	rs759997079
ensembl	rs759997079
geneview	rs759997079
scholar	rs759997079
google	rs759997079
pharmgkb	rs759997079
gwascentral	rs759997079
openSNP	rs759997079
23andMe	rs759997079
SNPshot	rs759997079
SNPdbe	rs759997079
MSV3d	rs759997079
GWAS Ctlg	rs759997079

Max Magnitude

0

ClinVar
Risk	rs759997079(G;G)
Alt	rs759997079(G;G)
Reference	Rs759997079(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MVK
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.110029079A>G
CLNSRC
CLNACC	RCV000213141.1,