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rs267607260

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607260(C;T)
Make rs267607260(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position27309934
GeneMPV17, UCN
is asnp
is mentioned by
dbSNPrs267607260
ebirs267607260
HLIrs267607260
Exacrs267607260
Varsomers267607260
Maprs267607260
PheGenIrs267607260
hapmaprs267607260
1000 genomesrs267607260
hgdprs267607260
ensemblrs267607260
gopubmedrs267607260
geneviewrs267607260
scholarrs267607260
googlers267607260
pharmgkbrs267607260
gwascentralrs267607260
openSNPrs267607260
23andMers267607260
23andMe allrs267607260
SNP Nexus

SNPshotrs267607260
SNPdbers267607260
MSV3drs267607260
GWAS Ctlgrs267607260
Max Magnitude0
ClinVar
Risk rs267607260(T;T)
Alt rs267607260(T;T)
Reference rs267607260(C;C)
Significance Pathogenic
Disease Navajo neurohepatopathy
Variation info
Gene UCN MPV17
CLNDBN Navajo neurohepatopathy
Reversed 1
HGVS NC_000002.11:g.27532802G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000031914.1,