rs879255651

Orientation

plus

Stabilized

plus

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

Make rs879255651(A;A)

Make rs879255651(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

3

Position

155116548

Gene

MME

is a	snp
is	mentioned by
dbSNP	rs879255651
dbSNP (classic)	rs879255651
ClinGen	rs879255651
ebi	rs879255651
HLI	rs879255651
Exac	rs879255651
Gnomad	rs879255651
Varsome	rs879255651
LitVar	rs879255651
Map	rs879255651
PheGenI	rs879255651
Biobank	rs879255651
1000 genomes	rs879255651
hgdp	rs879255651
ensembl	rs879255651
geneview	rs879255651
scholar	rs879255651
google	rs879255651
pharmgkb	rs879255651
gwascentral	rs879255651
openSNP	rs879255651
23andMe	rs879255651
SNPshot	rs879255651
SNPdbe	rs879255651
MSV3d	rs879255651
GWAS Ctlg	rs879255651

Max Magnitude

0

ClinVar
Risk	rs879255651(A;A)
Alt	rs879255651(A;A)
Reference	Rs879255651(G;G)
Significance	Pathogenic
Disease	Spinocerebellar ataxia 43
Variation	info
Gene	MME
CLNDBN	Spinocerebellar ataxia 43
Reversed	0
HGVS	NC_000003.11:g.154834337G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000239627.2,