rs387907022

Orientation

plus

Stabilized

plus

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

Make rs387907022(A;A)

Make rs387907022(A;G)

Reference

GRCh38 38.1/141

Chromosome

22

Position

46353829

Gene

TRMU

is a	snp
is	mentioned by
dbSNP	rs387907022
dbSNP (classic)	rs387907022
ClinGen	rs387907022
ebi	rs387907022
HLI	rs387907022
Exac	rs387907022
Gnomad	rs387907022
Varsome	rs387907022
LitVar	rs387907022
Map	rs387907022
PheGenI	rs387907022
Biobank	rs387907022
1000 genomes	rs387907022
hgdp	rs387907022
ensembl	rs387907022
geneview	rs387907022
scholar	rs387907022
google	rs387907022
pharmgkb	rs387907022
gwascentral	rs387907022
openSNP	rs387907022
23andMe	rs387907022
SNPshot	rs387907022
SNPdbe	rs387907022
MSV3d	rs387907022
GWAS Ctlg	rs387907022

Max Magnitude

0

ClinVar
Risk	rs387907022(A;A)
Alt	rs387907022(A;A)
Reference	Rs387907022(G;G)
Significance	Pathogenic
Disease	Liver failure acute infantile not provided
Variation	info
Gene	TRMU
CLNDBN	Liver failure acute infantile not provided
Reversed	0
HGVS	NC_000022.10:g.46749726G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023804.2, RCV000442392.1,