rs151249432

Orientation

plus

Stabilized

plus

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

Make rs151249432(C;T)

Make rs151249432(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

89550557

Gene

SPG7

is a	snp
is	mentioned by
dbSNP	rs151249432
dbSNP (classic)	rs151249432
ClinGen	rs151249432
ebi	rs151249432
HLI	rs151249432
Exac	rs151249432
Gnomad	rs151249432
Varsome	rs151249432
LitVar	rs151249432
Map	rs151249432
PheGenI	rs151249432
Biobank	rs151249432
1000 genomes	rs151249432
hgdp	rs151249432
ensembl	rs151249432
geneview	rs151249432
scholar	rs151249432
google	rs151249432
pharmgkb	rs151249432
gwascentral	rs151249432
openSNP	rs151249432
23andMe	rs151249432
SNPshot	rs151249432
SNPdbe	rs151249432
MSV3d	rs151249432
GWAS Ctlg	rs151249432

Max Magnitude

0

ClinVar
Risk	rs151249432(G;G) rs151249432(T;T)
Alt	rs151249432(G;G) rs151249432(T;T)
Reference	Rs151249432(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RPL13 SPG7
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.89616965C>G
CLNSRC
CLNACC	RCV000197553.2,