rs863223891

Orientation

minus

Stabilized

minus

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

Make rs863223891(A;A)

Make rs863223891(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

12356806

Gene

AFG3L2

is a	snp
is	mentioned by
dbSNP	rs863223891
dbSNP (classic)	rs863223891
ClinGen	rs863223891
ebi	rs863223891
HLI	rs863223891
Exac	rs863223891
Gnomad	rs863223891
Varsome	rs863223891
LitVar	rs863223891
Map	rs863223891
PheGenI	rs863223891
Biobank	rs863223891
1000 genomes	rs863223891
hgdp	rs863223891
ensembl	rs863223891
geneview	rs863223891
scholar	rs863223891
google	rs863223891
pharmgkb	rs863223891
gwascentral	rs863223891
openSNP	rs863223891
23andMe	rs863223891
SNPshot	rs863223891
SNPdbe	rs863223891
MSV3d	rs863223891
GWAS Ctlg	rs863223891

Max Magnitude

0

ClinVar
Risk	rs863223891(A;A)
Alt	rs863223891(A;A)
Reference	Rs863223891(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AFG3L2
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.12356805C>T
CLNSRC
CLNACC	RCV000199195.1,