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rs41362547

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs41362547(A;G)
Make rs41362547(G;G)
ReferenceGRCh37 37.1/132
ChromosomeMT
Position10044
GeneMT-TG
is asnp
is mentioned by
dbSNPrs41362547
ebirs41362547
HLIrs41362547
Exacrs41362547
Varsomers41362547
Maprs41362547
PheGenIrs41362547
hapmaprs41362547
1000 genomesrs41362547
hgdprs41362547
ensemblrs41362547
gopubmedrs41362547
geneviewrs41362547
scholarrs41362547
googlers41362547
pharmgkbrs41362547
gwascentralrs41362547
openSNPrs41362547
23andMers41362547
23andMe allrs41362547
SNP Nexus

SNPshotrs41362547
SNPdbers41362547
MSV3drs41362547
GWAS Ctlgrs41362547
GMAF0.003742
Max Magnitude0

haplogroups


ClinVar
Risk rs41362547(G;G)
Alt rs41362547(G;G)
Reference rs41362547(A;A)
Significance Pathogenic
Disease Sudden death
Variation info
Gene
CLNDBN Sudden death
Reversed 0
HGVS NC_012920.1:m.10044A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010237.2,