rs3774729

Orientation

plus

Stabilized

plus

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

Make rs3774729(A;A)

Make rs3774729(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

63996406

Gene

ATXN7

is a	snp
is	mentioned by
dbSNP	rs3774729
dbSNP (classic)	rs3774729
ClinGen	rs3774729
ebi	rs3774729
HLI	rs3774729
Exac	rs3774729
Gnomad	rs3774729
Varsome	rs3774729
LitVar	rs3774729
Map	rs3774729
PheGenI	rs3774729
Biobank	rs3774729
1000 genomes	rs3774729
hgdp	rs3774729
ensembl	rs3774729
geneview	rs3774729
scholar	rs3774729
google	rs3774729
pharmgkb	rs3774729
gwascentral	rs3774729
openSNP	rs3774729
23andMe	rs3774729
SNPshot	rs3774729
SNPdbe	rs3774729
MSV3d	rs3774729
GWAS Ctlg	rs3774729

GMAF

0.4362

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 23100044] Genetic Variation in Ataxia Gene ATXN7 Influences Cerebellar Grey Matter Volume in Healthy Adults

ClinVar
Risk	rs3774729(A;A) rs3774729(T;T)
Alt	rs3774729(A;A) rs3774729(T;T)
Reference	Rs3774729(G;G)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	ATXN7
CLNDBN	not specified
Reversed	0
HGVS	NC_000003.11:g.63982082G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000116488.2,