rs367683258

Orientation

plus

Stabilized

plus

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

Make rs367683258(C;T)

Make rs367683258(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

46352276

Gene

TRMU

is a	snp
is	mentioned by
dbSNP	rs367683258
dbSNP (classic)	rs367683258
ClinGen	rs367683258
ebi	rs367683258
HLI	rs367683258
Exac	rs367683258
Gnomad	rs367683258
Varsome	rs367683258
LitVar	rs367683258
Map	rs367683258
PheGenI	rs367683258
Biobank	rs367683258
1000 genomes	rs367683258
hgdp	rs367683258
ensembl	rs367683258
geneview	rs367683258
scholar	rs367683258
google	rs367683258
pharmgkb	rs367683258
gwascentral	rs367683258
openSNP	rs367683258
23andMe	rs367683258
SNPshot	rs367683258
SNPdbe	rs367683258
MSV3d	rs367683258
GWAS Ctlg	rs367683258

Max Magnitude

0

ClinVar
Risk	rs367683258(G;G) rs367683258(T;T)
Alt	rs367683258(G;G) rs367683258(T;T)
Reference	Rs367683258(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TRMU
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.46748173C>T
CLNSRC
CLNACC	RCV000200369.2,