rs1057519024

Orientation

plus

Stabilized

plus

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

Make rs1057519024(A;A)

Make rs1057519024(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

155116561

Gene

MME

is a	snp
is	mentioned by
dbSNP	rs1057519024
dbSNP (classic)	rs1057519024
ClinGen	rs1057519024
ebi	rs1057519024
HLI	rs1057519024
Exac	rs1057519024
Gnomad	rs1057519024
Varsome	rs1057519024
LitVar	rs1057519024
Map	rs1057519024
PheGenI	rs1057519024
Biobank	rs1057519024
1000 genomes	rs1057519024
hgdp	rs1057519024
ensembl	rs1057519024
geneview	rs1057519024
scholar	rs1057519024
google	rs1057519024
pharmgkb	rs1057519024
gwascentral	rs1057519024
openSNP	rs1057519024
23andMe	rs1057519024
SNPshot	rs1057519024
SNPdbe	rs1057519024
MSV3d	rs1057519024
GWAS Ctlg	rs1057519024

Max Magnitude

0

ClinVar
Risk	rs1057519024(A;A)
Alt	rs1057519024(A;A)
Reference	Rs1057519024(T;T)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	MME
CLNDBN	Charcot-Marie-Tooth disease, axonal, type 2T
Reversed	0
HGVS	NC_000003.11:g.154834350T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000234893.1,