Have questions? Visit https://www.reddit.com/r/SNPedia

rs28358582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28358582(C;C)
Make rs28358582(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position3308
GeneMT-ND1
is asnp
is mentioned by
dbSNPrs28358582
ebirs28358582
HLIrs28358582
Exacrs28358582
Varsomers28358582
Maprs28358582
PheGenIrs28358582
hapmaprs28358582
1000 genomesrs28358582
hgdprs28358582
ensemblrs28358582
gopubmedrs28358582
geneviewrs28358582
scholarrs28358582
googlers28358582
pharmgkbrs28358582
gwascentralrs28358582
openSNPrs28358582
23andMers28358582
23andMe allrs28358582
SNP Nexus

SNPshotrs28358582
SNPdbers28358582
MSV3drs28358582
GWAS Ctlgrs28358582
GMAF0.02713
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs28358582(A,C,G;A,C,G)
Alt rs28358582(A,C,G;A,C,G)
Reference rs28358582(T;T)
Significance Pathogenic
Disease Carcinoma of colon SUDDEN INFANT DEATH SYNDROME not specified
Variation info
Gene ND1
CLNDBN Carcinoma of colon SUDDEN INFANT DEATH SYNDROME not specified
Reversed 0
HGVS NC_012920.1:m.3308T>C; NC_012920.1:m.3308T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010379.2, RCV000010380.4, RCV000239184.1, RCV000010381.2,