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rs367838807

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs367838807(C;C)
Make rs367838807(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position27322498
GeneMPV17
is asnp
is mentioned by
dbSNPrs367838807
ebirs367838807
HLIrs367838807
Exacrs367838807
Varsomers367838807
Maprs367838807
PheGenIrs367838807
hapmaprs367838807
1000 genomesrs367838807
hgdprs367838807
ensemblrs367838807
gopubmedrs367838807
geneviewrs367838807
scholarrs367838807
googlers367838807
pharmgkbrs367838807
gwascentralrs367838807
openSNPrs367838807
23andMers367838807
23andMe allrs367838807
SNP Nexus

SNPshotrs367838807
SNPdbers367838807
MSV3drs367838807
GWAS Ctlgrs367838807
Max Magnitude0
ClinVar
Risk rs367838807(C;C)
Alt rs367838807(C;C)
Reference rs367838807(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MPV17
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.27545365T>C
CLNSRC
CLNACC RCV000199973.1,