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rs794729179

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729179(A;A)
Make rs794729179(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position14141692
GeneTMEM43
is asnp
is mentioned by
dbSNPrs794729179
ebirs794729179
HLIrs794729179
Exacrs794729179
Varsomers794729179
Maprs794729179
PheGenIrs794729179
hapmaprs794729179
1000 genomesrs794729179
hgdprs794729179
ensemblrs794729179
gopubmedrs794729179
geneviewrs794729179
scholarrs794729179
googlers794729179
pharmgkbrs794729179
gwascentralrs794729179
openSNPrs794729179
23andMers794729179
23andMe allrs794729179
SNP Nexus

SNPshotrs794729179
SNPdbers794729179
MSV3drs794729179
GWAS Ctlgrs794729179
Max Magnitude0
ClinVar
Risk rs794729179(A;A)
Alt rs794729179(A;A)
Reference rs794729179(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TMEM43
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.14183192G>A
CLNSRC
CLNACC RCV000183945.2,