Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607259

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607259(A;A)
Make rs267607259(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position27309958
GeneMPV17, UCN
is asnp
is mentioned by
dbSNPrs267607259
ebirs267607259
HLIrs267607259
Exacrs267607259
Varsomers267607259
Maprs267607259
PheGenIrs267607259
hapmaprs267607259
1000 genomesrs267607259
hgdprs267607259
ensemblrs267607259
gopubmedrs267607259
geneviewrs267607259
scholarrs267607259
googlers267607259
pharmgkbrs267607259
gwascentralrs267607259
openSNPrs267607259
23andMers267607259
23andMe allrs267607259
SNP Nexus

SNPshotrs267607259
SNPdbers267607259
MSV3drs267607259
GWAS Ctlgrs267607259
Max Magnitude0
ClinVar
Risk rs267607259(A;A)
Alt rs267607259(A;A)
Reference rs267607259(C;C)
Significance Pathogenic
Disease Navajo neurohepatopathy
Variation info
Gene UCN MPV17
CLNDBN Navajo neurohepatopathy
Reversed 1
HGVS NC_000002.11:g.27532826G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000031913.1,