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

rs267607257

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607257(C;C)
Make rs267607257(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position27312589
GeneMPV17
is asnp
is mentioned by
dbSNPrs267607257
ebirs267607257
HLIrs267607257
Exacrs267607257
Varsomers267607257
Maprs267607257
PheGenIrs267607257
hapmaprs267607257
1000 genomesrs267607257
hgdprs267607257
ensemblrs267607257
gopubmedrs267607257
geneviewrs267607257
scholarrs267607257
googlers267607257
pharmgkbrs267607257
gwascentralrs267607257
openSNPrs267607257
23andMers267607257
23andMe allrs267607257
SNP Nexus

SNPshotrs267607257
SNPdbers267607257
MSV3drs267607257
GWAS Ctlgrs267607257
Max Magnitude0
ClinVar
Risk rs267607257(C;C)
Alt rs267607257(C;C)
Reference rs267607257(G;G)
Significance Pathogenic
Disease Navajo neurohepatopathy
Variation info
Gene MPV17
CLNDBN Navajo neurohepatopathy
Reversed 1
HGVS NC_000002.11:g.27535456C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000031910.1,