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rs267607263

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs267607263(-;-)
Make rs267607263(-;AGA)
ReferenceGRCh38 38.1/141
Chromosome2
Position27312694
GeneMPV17
is asnp
is mentioned by
dbSNPrs267607263
ebirs267607263
HLIrs267607263
Exacrs267607263
Varsomers267607263
Maprs267607263
PheGenIrs267607263
hapmaprs267607263
1000 genomesrs267607263
hgdprs267607263
ensemblrs267607263
gopubmedrs267607263
geneviewrs267607263
scholarrs267607263
googlers267607263
pharmgkbrs267607263
gwascentralrs267607263
openSNPrs267607263
23andMers267607263
23andMe allrs267607263
SNP Nexus

SNPshotrs267607263
SNPdbers267607263
MSV3drs267607263
GWAS Ctlgrs267607263
Max Magnitude0
ClinVar
Risk rs267607263(;)
Alt rs267607263(;)
Reference rs267607263(AGA;AGA)
Significance Pathogenic
Disease Navajo neurohepatopathy not provided
Variation info
Gene MPV17
CLNDBN Navajo neurohepatopathy not provided
Reversed 1
HGVS NC_000002.11:g.27535561_27535563delTCT
CLNSRC ClinVar GeneReviews
CLNACC RCV000031908.1, RCV000197566.1,