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rs267607261

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607261(A;A)
Make rs267607261(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position27312753
GeneMPV17
is asnp
is mentioned by
dbSNPrs267607261
ebirs267607261
HLIrs267607261
Exacrs267607261
Varsomers267607261
Maprs267607261
PheGenIrs267607261
hapmaprs267607261
1000 genomesrs267607261
hgdprs267607261
ensemblrs267607261
gopubmedrs267607261
geneviewrs267607261
scholarrs267607261
googlers267607261
pharmgkbrs267607261
gwascentralrs267607261
openSNPrs267607261
23andMers267607261
23andMe allrs267607261
SNP Nexus

SNPshotrs267607261
SNPdbers267607261
MSV3drs267607261
GWAS Ctlgrs267607261
Max Magnitude0
ClinVar
Risk rs267607261(A;A)
Alt rs267607261(A;A)
Reference rs267607261(G;G)
Significance Pathogenic
Disease Navajo neurohepatopathy
Variation info
Gene MPV17
CLNDBN Navajo neurohepatopathy
Reversed 1
HGVS NC_000002.11:g.27535620C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000031904.1,