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rs267607266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607266(-;-)
Make rs267607266(-;C)
Make rs267607266(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position27322495
GeneMPV17
is asnp
is mentioned by
dbSNPrs267607266
ebirs267607266
HLIrs267607266
Exacrs267607266
Varsomers267607266
Maprs267607266
PheGenIrs267607266
hapmaprs267607266
1000 genomesrs267607266
hgdprs267607266
ensemblrs267607266
gopubmedrs267607266
geneviewrs267607266
scholarrs267607266
googlers267607266
pharmgkbrs267607266
gwascentralrs267607266
openSNPrs267607266
23andMers267607266
23andMe allrs267607266
SNP Nexus

SNPshotrs267607266
SNPdbers267607266
MSV3drs267607266
GWAS Ctlgrs267607266
Max Magnitude0
ClinVar
Risk rs267607266(C;C)
Alt rs267607266(C;C)
Reference rs267607266(;)
Significance Pathogenic
Disease Navajo neurohepatopathy
Variation info
Gene MPV17
CLNDBN Navajo neurohepatopathy
Reversed 1
HGVS NC_000002.11:g.27545363dupG
CLNSRC ClinVar GeneReviews
CLNACC RCV000031905.1,