rs779805236

Orientation

plus

Stabilized

plus

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

Make rs779805236(A;G)

Make rs779805236(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

12370847

Gene

AFG3L2

is a	snp
is	mentioned by
dbSNP	rs779805236
dbSNP (classic)	rs779805236
ClinGen	rs779805236
ebi	rs779805236
HLI	rs779805236
Exac	rs779805236
Gnomad	rs779805236
Varsome	rs779805236
LitVar	rs779805236
Map	rs779805236
PheGenI	rs779805236
Biobank	rs779805236
1000 genomes	rs779805236
hgdp	rs779805236
ensembl	rs779805236
geneview	rs779805236
scholar	rs779805236
google	rs779805236
pharmgkb	rs779805236
gwascentral	rs779805236
openSNP	rs779805236
23andMe	rs779805236
SNPshot	rs779805236
SNPdbe	rs779805236
MSV3d	rs779805236
GWAS Ctlg	rs779805236

Max Magnitude

0

ClinVar
Risk	rs779805236(G;G)
Alt	rs779805236(G;G)
Reference	Rs779805236(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AFG3L2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.12370846A>G
CLNSRC
CLNACC	RCV000482350.1,