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rs376589026

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376589026(G;T)
Make rs376589026(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position14139302
GeneTMEM43
is asnp
is mentioned by
dbSNPrs376589026
ebirs376589026
HLIrs376589026
Exacrs376589026
Varsomers376589026
Maprs376589026
PheGenIrs376589026
hapmaprs376589026
1000 genomesrs376589026
hgdprs376589026
ensemblrs376589026
gopubmedrs376589026
geneviewrs376589026
scholarrs376589026
googlers376589026
pharmgkbrs376589026
gwascentralrs376589026
openSNPrs376589026
23andMers376589026
23andMe allrs376589026
SNP Nexus

SNPshotrs376589026
SNPdbers376589026
MSV3drs376589026
GWAS Ctlgrs376589026
Max Magnitude0
ClinVar
Risk rs376589026(T;T)
Alt rs376589026(T;T)
Reference rs376589026(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TMEM43
CLNDBN not specified not provided
Reversed 0
HGVS NC_000003.11:g.14180802G>T
CLNSRC
CLNACC RCV000039374.2, RCV000183943.1,