rs1005670966

Orientation

plus

Stabilized

plus

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

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

12351097

Gene

AFG3L2

is a	snp
is	mentioned by
dbSNP	rs1005670966
dbSNP (classic)	rs1005670966
ClinGen	rs1005670966
ebi	rs1005670966
HLI	rs1005670966
Exac	rs1005670966
Gnomad	rs1005670966
Varsome	rs1005670966
LitVar	rs1005670966
Map	rs1005670966
PheGenI	rs1005670966
Biobank	rs1005670966
1000 genomes	rs1005670966
hgdp	rs1005670966
ensembl	rs1005670966
geneview	rs1005670966
scholar	rs1005670966
google	rs1005670966
pharmgkb	rs1005670966
gwascentral	rs1005670966
openSNP	rs1005670966
23andMe	rs1005670966
SNPshot	rs1005670966
SNPdbe	rs1005670966
MSV3d	rs1005670966
GWAS Ctlg	rs1005670966

Max Magnitude

0

ClinVar
Risk	rs1005670966(A;A)
Alt	rs1005670966(A;A)
Reference	Rs1005670966(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AFG3L2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.12351096G>A
CLNSRC
CLNACC	RCV000489336.1,