rs80338928

Orientation

minus

Stabilized

minus

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

Make rs80338928(-;-)

Make rs80338928(-;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

149027541

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs80338928
dbSNP (classic)	rs80338928
ClinGen	rs80338928
ebi	rs80338928
HLI	rs80338928
Exac	rs80338928
Gnomad	rs80338928
Varsome	rs80338928
LitVar	rs80338928
Map	rs80338928
PheGenI	rs80338928
Biobank	rs80338928
1000 genomes	rs80338928
hgdp	rs80338928
ensembl	rs80338928
geneview	rs80338928
scholar	rs80338928
google	rs80338928
pharmgkb	rs80338928
gwascentral	rs80338928
openSNP	rs80338928
23andMe	rs80338928
SNPshot	rs80338928
SNPdbe	rs80338928
MSV3d	rs80338928
GWAS Ctlg	rs80338928

Max Magnitude

0

ClinVar
Risk	rs80338928(-;-)
Alt	rs80338928(-;-)
Reference	Rs80338928(G;G)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	SH3TC2
CLNDBN	Charcot-Marie-Tooth disease, type 4C
Reversed	1
HGVS	NC_000005.9:g.148407104delC
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020891.1,