rs587777838

Orientation

plus

Stabilized

plus

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

Make rs587777838(-;-)

Make rs587777838(-;A)

Reference

GRCh38 38.1/142

Chromosome

4

Position

153315998

Gene

TRIM2

is a	snp
is	mentioned by
dbSNP	rs587777838
dbSNP (classic)	rs587777838
ClinGen	rs587777838
ebi	rs587777838
HLI	rs587777838
Exac	rs587777838
Gnomad	rs587777838
Varsome	rs587777838
LitVar	rs587777838
Map	rs587777838
PheGenI	rs587777838
Biobank	rs587777838
1000 genomes	rs587777838
hgdp	rs587777838
ensembl	rs587777838
geneview	rs587777838
scholar	rs587777838
google	rs587777838
pharmgkb	rs587777838
gwascentral	rs587777838
openSNP	rs587777838
23andMe	rs587777838
SNPshot	rs587777838
SNPdbe	rs587777838
MSV3d	rs587777838
GWAS Ctlg	rs587777838

Max Magnitude

0

ClinVar
Risk	rs587777838(-;-)
Alt	rs587777838(-;-)
Reference	Rs587777838(A;A)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	TRIM2
CLNDBN	Charcot-Marie-Tooth disease, axonal, type 2R
Reversed	0
HGVS	NC_000004.11:g.154237150delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000074303.4,