rs80338935

Orientation

minus

Stabilized

minus

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

Make rs80338935(C;C)

Make rs80338935(C;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

149010271

Gene

SH3TC2

is a	snp
is	mentioned by
dbSNP	rs80338935
dbSNP (classic)	rs80338935
ClinGen	rs80338935
ebi	rs80338935
HLI	rs80338935
Exac	rs80338935
Gnomad	rs80338935
Varsome	rs80338935
LitVar	rs80338935
Map	rs80338935
PheGenI	rs80338935
Biobank	rs80338935
1000 genomes	rs80338935
hgdp	rs80338935
ensembl	rs80338935
geneview	rs80338935
scholar	rs80338935
google	rs80338935
pharmgkb	rs80338935
gwascentral	rs80338935
openSNP	rs80338935
23andMe	rs80338935
SNPshot	rs80338935
SNPdbe	rs80338935
MSV3d	rs80338935
GWAS Ctlg	rs80338935

Max Magnitude

0

ClinVar
Risk	rs80338935(A;A) rs80338935(C;C)
Alt	rs80338935(A;A) rs80338935(C;C)
Reference	Rs80338935(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.148389834C>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020896.1,