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rs139625465

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139625465(G;T)
Make rs139625465(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position7932691
GeneTIMM44
is asnp
is mentioned by
dbSNPrs139625465
ebirs139625465
HLIrs139625465
Exacrs139625465
Varsomers139625465
Maprs139625465
PheGenIrs139625465
hapmaprs139625465
1000 genomesrs139625465
hgdprs139625465
ensemblrs139625465
gopubmedrs139625465
geneviewrs139625465
scholarrs139625465
googlers139625465
pharmgkbrs139625465
gwascentralrs139625465
openSNPrs139625465
23andMers139625465
23andMe allrs139625465
SNP Nexus

SNPshotrs139625465
SNPdbers139625465
MSV3drs139625465
GWAS Ctlgrs139625465
Max Magnitude0
ClinVar
Risk rs139625465(A,T;A,T)
Alt rs139625465(A,T;A,T)
Reference rs139625465(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TIMM44
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.7997576G>T
CLNSRC
CLNACC RCV000198581.2,