rs149428

Orientation

plus

Stabilized

plus

Make rs149428(A;A)

Make rs149428(A;G)

Make rs149428(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

58634662

is a	snp
is	mentioned by
dbSNP	rs149428
dbSNP (classic)	rs149428
ClinGen	rs149428
ebi	rs149428
HLI	rs149428
Exac	rs149428
Gnomad	rs149428
Varsome	rs149428
LitVar	rs149428
Map	rs149428
PheGenI	rs149428
Biobank	rs149428
1000 genomes	rs149428
hgdp	rs149428
ensembl	rs149428
geneview	rs149428
scholar	rs149428
google	rs149428
pharmgkb	rs149428
gwascentral	rs149428
openSNP	rs149428
23andMe	rs149428
SNPshot	rs149428
SNPdbe	rs149428
MSV3d	rs149428
GWAS Ctlg	rs149428

GMAF

0.1983

Max Magnitude

0

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

OMIM	612319
Desc	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE; SPG35
Variant
Related	also

[PMID 18463364] A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.