rs139469785

Orientation

plus

Stabilized

plus

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

Make rs139469785(C;T)

Make rs139469785(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

12337349

Gene	AFG3L2, LOC107985154

is a	snp
is	mentioned by
dbSNP	rs139469785
dbSNP (classic)	rs139469785
ClinGen	rs139469785
ebi	rs139469785
HLI	rs139469785
Exac	rs139469785
Gnomad	rs139469785
Varsome	rs139469785
LitVar	rs139469785
Map	rs139469785
PheGenI	rs139469785
Biobank	rs139469785
1000 genomes	rs139469785
hgdp	rs139469785
ensembl	rs139469785
geneview	rs139469785
scholar	rs139469785
google	rs139469785
pharmgkb	rs139469785
gwascentral	rs139469785
openSNP	rs139469785
23andMe	rs139469785
SNPshot	rs139469785
SNPdbe	rs139469785
MSV3d	rs139469785
GWAS Ctlg	rs139469785

Max Magnitude

0

ClinVar
Risk	rs139469785(T;T)
Alt	rs139469785(T;T)
Reference	Rs139469785(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AFG3L2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.12337348C>T
CLNSRC
CLNACC	RCV000195592.2,