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rs765987297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs765987297(-;-)
Make rs765987297(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position12337448
GeneAFG3L2, LOC107985154
is asnp
is mentioned by
dbSNPrs765987297
dbSNP (old)rs765987297
ClinGenrs765987297
ebirs765987297
HLIrs765987297
Exacrs765987297
Gnomadrs765987297
Varsomers765987297
Maprs765987297
PheGenIrs765987297
Biobankrs765987297
1000 genomesrs765987297
hgdprs765987297
ensemblrs765987297
gopubmedrs765987297
geneviewrs765987297
scholarrs765987297
googlers765987297
pharmgkbrs765987297
gwascentralrs765987297
openSNPrs765987297
23andMers765987297
23andMe allrs765987297
SNP Nexus

SNPshotrs765987297
SNPdbers765987297
MSV3drs765987297
GWAS Ctlgrs765987297
Max Magnitude0
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,