rs864622664

Orientation

minus

Stabilized

minus

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

Make rs864622664(-;-)

Make rs864622664(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

149010294

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs864622664
dbSNP (classic)	rs864622664
ClinGen	rs864622664
ebi	rs864622664
HLI	rs864622664
Exac	rs864622664
Gnomad	rs864622664
Varsome	rs864622664
LitVar	rs864622664
Map	rs864622664
PheGenI	rs864622664
Biobank	rs864622664
1000 genomes	rs864622664
hgdp	rs864622664
ensembl	rs864622664
geneview	rs864622664
scholar	rs864622664
google	rs864622664
pharmgkb	rs864622664
gwascentral	rs864622664
openSNP	rs864622664
23andMe	rs864622664
SNPshot	rs864622664
SNPdbe	rs864622664
MSV3d	rs864622664
GWAS Ctlg	rs864622664

Max Magnitude

0

ClinVar
Risk	rs864622664(-;-)
Alt	rs864622664(-;-)
Reference	Rs864622664(G;G)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease not provided
Variation	info
Gene	SH3TC2
CLNDBN	Charcot-Marie-Tooth disease, type IV not provided
Reversed	1
HGVS	NC_000005.9:g.148389857delC
CLNSRC
CLNACC	RCV000205253.1, RCV000484617.1,