rs878855083

Orientation

minus

Stabilized

minus

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

Make rs878855083(-;-)

Make rs878855083(-;CT)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

74716564

Gene

FA2H

is a	snp
is	mentioned by
dbSNP	rs878855083
dbSNP (classic)	rs878855083
ClinGen	rs878855083
ebi	rs878855083
HLI	rs878855083
Exac	rs878855083
Gnomad	rs878855083
Varsome	rs878855083
LitVar	rs878855083
Map	rs878855083
PheGenI	rs878855083
Biobank	rs878855083
1000 genomes	rs878855083
hgdp	rs878855083
ensembl	rs878855083
geneview	rs878855083
scholar	rs878855083
google	rs878855083
pharmgkb	rs878855083
gwascentral	rs878855083
openSNP	rs878855083
23andMe	rs878855083
SNPshot	rs878855083
SNPdbe	rs878855083
MSV3d	rs878855083
GWAS Ctlg	rs878855083

Max Magnitude

0

ClinVar
Risk	rs878855083(-;-)
Alt	rs878855083(-;-)
Reference	Rs878855083(CT;CT)
Significance	Pathogenic
Disease	Spastic paraplegia
Variation	info
Gene	FA2H
CLNDBN	Spastic paraplegia
Reversed	1
HGVS	NC_000016.9:g.74750462_74750463delAG
CLNSRC
CLNACC	RCV000225829.1,