rs863224870

Orientation

minus

Stabilized

minus

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

Make rs863224870(C;T)

Make rs863224870(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

74726321

Gene

FA2H

is a	snp
is	mentioned by
dbSNP	rs863224870
dbSNP (classic)	rs863224870
ClinGen	rs863224870
ebi	rs863224870
HLI	rs863224870
Exac	rs863224870
Gnomad	rs863224870
Varsome	rs863224870
LitVar	rs863224870
Map	rs863224870
PheGenI	rs863224870
Biobank	rs863224870
1000 genomes	rs863224870
hgdp	rs863224870
ensembl	rs863224870
geneview	rs863224870
scholar	rs863224870
google	rs863224870
pharmgkb	rs863224870
gwascentral	rs863224870
openSNP	rs863224870
23andMe	rs863224870
SNPshot	rs863224870
SNPdbe	rs863224870
MSV3d	rs863224870
GWAS Ctlg	rs863224870

Max Magnitude

0

ClinVar
Risk	rs863224870(T;T)
Alt	rs863224870(T;T)
Reference	Rs863224870(C;C)
Significance	Probable-Pathogenic
Disease	Spastic paraplegia 35
Variation	info
Gene	FA2H
CLNDBN	Spastic paraplegia 35
Reversed	1
HGVS	NC_000016.9:g.74760219G>A
CLNSRC
CLNACC	RCV000199368.1,