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rs41456348

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41456348(C;C)
Make rs41456348(C;T)
ReferenceGRCh37 37.1/132
ChromosomeMT
Position4336
GeneMT-TQ
is asnp
is mentioned by
dbSNPrs41456348
ebirs41456348
HLIrs41456348
Exacrs41456348
Varsomers41456348
Maprs41456348
PheGenIrs41456348
hapmaprs41456348
1000 genomesrs41456348
hgdprs41456348
ensemblrs41456348
gopubmedrs41456348
geneviewrs41456348
scholarrs41456348
googlers41456348
pharmgkbrs41456348
gwascentralrs41456348
openSNPrs41456348
23andMers41456348
23andMe allrs41456348
SNP Nexus

SNPshotrs41456348
SNPdbers41456348
MSV3drs41456348
GWAS Ctlgrs41456348
Merged fromRs45517935
GMAF0.009355
Max Magnitude0

is a mitochondrial


ClinVar
Risk rs41456348(C;C)
Alt rs41456348(C;C)
Reference rs41456348(T;T)
Significance Pathogenic
Disease Sensorineural deafness and migraine not provided
Variation info
Gene
CLNDBN Sensorineural deafness and migraine not provided
Reversed 0
HGVS NC_012920.1:m.4336T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010239.2, RCV000224964.1,