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rs267607267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607267(-;-)
Make rs267607267(-;C)
Make rs267607267(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position27311908
GeneMPV17
is asnp
is mentioned by
dbSNPrs267607267
ebirs267607267
HLIrs267607267
Exacrs267607267
Varsomers267607267
Maprs267607267
PheGenIrs267607267
hapmaprs267607267
1000 genomesrs267607267
hgdprs267607267
ensemblrs267607267
gopubmedrs267607267
geneviewrs267607267
scholarrs267607267
googlers267607267
pharmgkbrs267607267
gwascentralrs267607267
openSNPrs267607267
23andMers267607267
23andMe allrs267607267
SNP Nexus

SNPshotrs267607267
SNPdbers267607267
MSV3drs267607267
GWAS Ctlgrs267607267
Max Magnitude0
ClinVar
Risk rs267607267(C;C)
Alt rs267607267(C;C)
Reference rs267607267(;)
Significance Pathogenic
Disease Navajo neurohepatopathy
Variation info
Gene MPV17
CLNDBN Navajo neurohepatopathy
Reversed 1
HGVS NC_000002.11:g.27534777dupG
CLNSRC ClinVar GeneReviews
CLNACC RCV000031912.1,