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rs1043953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1043953(A;G)
Make rs1043953(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position14142258
GeneTMEM43
is asnp
is mentioned by
dbSNPrs1043953
dbSNP (old)rs1043953
ClinGenrs1043953
ebirs1043953
HLIrs1043953
Exacrs1043953
Gnomadrs1043953
Varsomers1043953
Maprs1043953
PheGenIrs1043953
Biobankrs1043953
1000 genomesrs1043953
hgdprs1043953
ensemblrs1043953
gopubmedrs1043953
geneviewrs1043953
scholarrs1043953
googlers1043953
pharmgkbrs1043953
gwascentralrs1043953
openSNPrs1043953
23andMers1043953
23andMe allrs1043953
SNP Nexus

SNPshotrs1043953
SNPdbers1043953
MSV3drs1043953
GWAS Ctlgrs1043953
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 25778469OA-icon.png] Genetic variants in DNA repair genes as potential predictive markers for oxaliplatin chemotherapy in colorectal cancer


ClinVar
Risk rs1043953(G;G)
Alt rs1043953(G;G)
Reference Rs1043953(A;A)
Significance Probable-non-pathogenic
Disease Cardiomyopathy Xeroderma pigmentosum
Variation info
Gene TMEM43
CLNDBN Cardiomyopathy, ARVC Xeroderma pigmentosum
Reversed 0
HGVS NC_000003.11:g.14183758A>G
CLNSRC
CLNACC RCV000284996.1, RCV000295901.1,