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rs863224074

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224074(C;T)
Make rs863224074(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position27312499
GeneMPV17
is asnp
is mentioned by
dbSNPrs863224074
ebirs863224074
HLIrs863224074
Exacrs863224074
Varsomers863224074
Maprs863224074
PheGenIrs863224074
hapmaprs863224074
1000 genomesrs863224074
hgdprs863224074
ensemblrs863224074
gopubmedrs863224074
geneviewrs863224074
scholarrs863224074
googlers863224074
pharmgkbrs863224074
gwascentralrs863224074
openSNPrs863224074
23andMers863224074
23andMe allrs863224074
SNP Nexus

SNPshotrs863224074
SNPdbers863224074
MSV3drs863224074
GWAS Ctlgrs863224074
Max Magnitude0
ClinVar
Risk rs863224074(T;T)
Alt rs863224074(T;T)
Reference rs863224074(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MPV17
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.27535366G>A
CLNSRC
CLNACC RCV000196530.1,