rs864622663

Orientation

minus

Stabilized

minus

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

Make rs864622663(C;T)

Make rs864622663(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

149047930

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs864622663
dbSNP (classic)	rs864622663
ClinGen	rs864622663
ebi	rs864622663
HLI	rs864622663
Exac	rs864622663
Gnomad	rs864622663
Varsome	rs864622663
LitVar	rs864622663
Map	rs864622663
PheGenI	rs864622663
Biobank	rs864622663
1000 genomes	rs864622663
hgdp	rs864622663
ensembl	rs864622663
geneview	rs864622663
scholar	rs864622663
google	rs864622663
pharmgkb	rs864622663
gwascentral	rs864622663
openSNP	rs864622663
23andMe	rs864622663
SNPshot	rs864622663
SNPdbe	rs864622663
MSV3d	rs864622663
GWAS Ctlg	rs864622663

Max Magnitude

0

ClinVar
Risk	rs864622663(T;T)
Alt	rs864622663(T;T)
Reference	Rs864622663(C;C)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	SH3TC2
CLNDBN	Charcot-Marie-Tooth disease, type IV
Reversed	1
HGVS	NC_000005.9:g.148427493G>A
CLNSRC
CLNACC	RCV000203755.1,