rs765987297

Orientation

plus

Stabilized

plus

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

Make rs765987297(-;-)

Make rs765987297(-;TG)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

12337448

Gene	AFG3L2, LOC107985154

is a	snp
is	mentioned by
dbSNP	rs765987297
dbSNP (classic)	rs765987297
ClinGen	rs765987297
ebi	rs765987297
HLI	rs765987297
Exac	rs765987297
Gnomad	rs765987297
Varsome	rs765987297
LitVar	rs765987297
Map	rs765987297
PheGenI	rs765987297
Biobank	rs765987297
1000 genomes	rs765987297
hgdp	rs765987297
ensembl	rs765987297
geneview	rs765987297
scholar	rs765987297
google	rs765987297
pharmgkb	rs765987297
gwascentral	rs765987297
openSNP	rs765987297
23andMe	rs765987297
SNPshot	rs765987297
SNPdbe	rs765987297
MSV3d	rs765987297
GWAS Ctlg	rs765987297

Max Magnitude

0

ClinVar
Risk	rs765987297(-;-)
Alt	rs765987297(-;-)
Reference	Rs765987297(TG;TG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	AFG3L2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.12337447_12337448delTG
CLNSRC
CLNACC	RCV000195472.1,