rs267607259

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs267607259(A;A)

Make rs267607259(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

27309958

Gene	MPV17, UCN

is a	snp
is	mentioned by
dbSNP	rs267607259
dbSNP (classic)	rs267607259
ClinGen	rs267607259
ebi	rs267607259
HLI	rs267607259
Exac	rs267607259
Gnomad	rs267607259
Varsome	rs267607259
LitVar	rs267607259
Map	rs267607259
PheGenI	rs267607259
Biobank	rs267607259
1000 genomes	rs267607259
hgdp	rs267607259
ensembl	rs267607259
geneview	rs267607259
scholar	rs267607259
google	rs267607259
pharmgkb	rs267607259
gwascentral	rs267607259
openSNP	rs267607259
23andMe	rs267607259
SNPshot	rs267607259
SNPdbe	rs267607259
MSV3d	rs267607259
GWAS Ctlg	rs267607259

Max Magnitude

0

ClinVar
Risk	rs267607259(A;A)
Alt	rs267607259(A;A)
Reference	Rs267607259(C;C)
Significance	Pathogenic
Disease	Navajo neurohepatopathy
Variation	info
Gene	UCN MPV17
CLNDBN	Navajo neurohepatopathy
Reversed	1
HGVS	NC_000002.11:g.27532826G>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000031913.1,