rs863223889

Orientation

minus

Stabilized

minus

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

Make rs863223889(A;A)

Make rs863223889(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

12358684

Gene

AFG3L2

is a	snp
is	mentioned by
dbSNP	rs863223889
dbSNP (classic)	rs863223889
ClinGen	rs863223889
ebi	rs863223889
HLI	rs863223889
Exac	rs863223889
Gnomad	rs863223889
Varsome	rs863223889
LitVar	rs863223889
Map	rs863223889
PheGenI	rs863223889
Biobank	rs863223889
1000 genomes	rs863223889
hgdp	rs863223889
ensembl	rs863223889
geneview	rs863223889
scholar	rs863223889
google	rs863223889
pharmgkb	rs863223889
gwascentral	rs863223889
openSNP	rs863223889
23andMe	rs863223889
SNPshot	rs863223889
SNPdbe	rs863223889
MSV3d	rs863223889
GWAS Ctlg	rs863223889

Max Magnitude

0

ClinVar
Risk	rs863223889(A;A)
Alt	rs863223889(A;A)
Reference	Rs863223889(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AFG3L2
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.12358683C>T
CLNSRC
CLNACC	RCV000198799.1,