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rs267607258

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607258(C;T)
Make rs267607258(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position27312576
GeneMPV17
is asnp
is mentioned by
dbSNPrs267607258
ebirs267607258
HLIrs267607258
Exacrs267607258
Varsomers267607258
Maprs267607258
PheGenIrs267607258
hapmaprs267607258
1000 genomesrs267607258
hgdprs267607258
ensemblrs267607258
gopubmedrs267607258
geneviewrs267607258
scholarrs267607258
googlers267607258
pharmgkbrs267607258
gwascentralrs267607258
openSNPrs267607258
23andMers267607258
23andMe allrs267607258
SNP Nexus

SNPshotrs267607258
SNPdbers267607258
MSV3drs267607258
GWAS Ctlgrs267607258
Max Magnitude0
ClinVar
Risk rs267607258(T;T)
Alt rs267607258(T;T)
Reference rs267607258(C;C)
Significance Pathogenic
Disease Navajo neurohepatopathy not provided
Variation info
Gene MPV17
CLNDBN Navajo neurohepatopathy not provided
Reversed 1
HGVS NC_000002.11:g.27535443G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000031911.1, RCV000198122.2,