rs587777315

Orientation

plus

Stabilized

plus

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

Make rs587777315(C;G)

Make rs587777315(G;G)

Reference

GRCh38 38.1/142

Chromosome

15

Position

64974732

Gene

SPG21

is a	snp
is	mentioned by
dbSNP	rs587777315
dbSNP (classic)	rs587777315
ClinGen	rs587777315
ebi	rs587777315
HLI	rs587777315
Exac	rs587777315
Gnomad	rs587777315
Varsome	rs587777315
LitVar	rs587777315
Map	rs587777315
PheGenI	rs587777315
Biobank	rs587777315
1000 genomes	rs587777315
hgdp	rs587777315
ensembl	rs587777315
geneview	rs587777315
scholar	rs587777315
google	rs587777315
pharmgkb	rs587777315
gwascentral	rs587777315
openSNP	rs587777315
23andMe	rs587777315
SNPshot	rs587777315
SNPdbe	rs587777315
MSV3d	rs587777315
GWAS Ctlg	rs587777315

Max Magnitude

0

ClinVar
Risk	rs587777315(G;G) rs587777315(T;T)
Alt	rs587777315(G;G) rs587777315(T;T)
Reference	Rs587777315(C;C)
Significance	Pathogenic
Disease	Mast syndrome
Variation	info
Gene	SPG21
CLNDBN	Mast syndrome
Reversed	0
HGVS	NC_000015.9:g.65267070C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000114945.2,