rs878855013

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;G)	3	Carrier of a spastic paraplegia type 15 mutation
(G;G)	0	common in clinvar

Make rs878855013(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

67769731

Gene

ZFYVE26

is a	snp
is	mentioned by
dbSNP	rs878855013
dbSNP (classic)	rs878855013
ClinGen	rs878855013
ebi	rs878855013
HLI	rs878855013
Exac	rs878855013
Gnomad	rs878855013
Varsome	rs878855013
LitVar	rs878855013
Map	rs878855013
PheGenI	rs878855013
Biobank	rs878855013
1000 genomes	rs878855013
hgdp	rs878855013
ensembl	rs878855013
geneview	rs878855013
scholar	rs878855013
google	rs878855013
pharmgkb	rs878855013
gwascentral	rs878855013
openSNP	rs878855013
23andMe	rs878855013
SNPshot	rs878855013
SNPdbe	rs878855013
MSV3d	rs878855013
GWAS Ctlg	rs878855013

Max Magnitude

3

aka c.5485-1delG

see ZFYVE26

ClinVar
Risk	rs878855013(-;-)
Alt	rs878855013(-;-)
Reference	Rs878855013(G;G)
Significance	Pathogenic
Disease	Spastic paraplegia Spastic paraplegia 15
Variation	info
Gene	ZFYVE26
CLNDBN	Spastic paraplegia Spastic paraplegia 15
Reversed	1
HGVS	NC_000014.8:g.68236448delC
CLNSRC
CLNACC	RCV000227299.1, RCV000330118.1,