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rs758026399

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758026399(C;T)
Make rs758026399(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position109586765
GeneMVK
is asnp
is mentioned by
dbSNPrs758026399
ebirs758026399
HLIrs758026399
Exacrs758026399
Varsomers758026399
Maprs758026399
PheGenIrs758026399
hapmaprs758026399
1000 genomesrs758026399
hgdprs758026399
ensemblrs758026399
gopubmedrs758026399
geneviewrs758026399
scholarrs758026399
googlers758026399
pharmgkbrs758026399
gwascentralrs758026399
openSNPrs758026399
23andMers758026399
23andMe allrs758026399
SNP Nexus

SNPshotrs758026399
SNPdbers758026399
MSV3drs758026399
GWAS Ctlgrs758026399
Max Magnitude0
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,