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rs759997079

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs759997079(A;G)
Make rs759997079(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position109591274
GeneMVK
is asnp
is mentioned by
dbSNPrs759997079
ebirs759997079
HLIrs759997079
Exacrs759997079
Varsomers759997079
Maprs759997079
PheGenIrs759997079
hapmaprs759997079
1000 genomesrs759997079
hgdprs759997079
ensemblrs759997079
gopubmedrs759997079
geneviewrs759997079
scholarrs759997079
googlers759997079
pharmgkbrs759997079
gwascentralrs759997079
openSNPrs759997079
23andMers759997079
23andMe allrs759997079
SNP Nexus

SNPshotrs759997079
SNPdbers759997079
MSV3drs759997079
GWAS Ctlgrs759997079
Max Magnitude0
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,