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rs2001030

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(G;G) 0 common on affy axiom data
Make rs2001030(A;G)
ReferenceGRCh37 37.1/132
ChromosomeMT
Position1438
GeneMT-RNR1
is asnp
is mentioned by
dbSNPrs2001030
ebirs2001030
HLIrs2001030
Exacrs2001030
Varsomers2001030
Maprs2001030
PheGenIrs2001030
hapmaprs2001030
1000 genomesrs2001030
hgdprs2001030
ensemblrs2001030
gopubmedrs2001030
geneviewrs2001030
scholarrs2001030
googlers2001030
pharmgkbrs2001030
gwascentralrs2001030
openSNPrs2001030
23andMers2001030
23andMe allrs2001030
SNP Nexus

SNPshotrs2001030
SNPdbers2001030
MSV3drs2001030
GWAS Ctlgrs2001030
GMAF0.04397
Max Magnitude0
? (A;A) (A;G) (G;G) 28
haplogroups


Haplogroup SNP
Alt. Name(s) G1438A
Source(s) [PMID 17099056]
Tree PhyloTree build 7
Clade
Haplogroup
No Clade Haplogroup
Ancestral
Haplogroup
Haplogroup H (mtDNA)
Derived
Haplogroup
Haplogroup H2 (mtDNA)
Ancestral Allele G
Derived Allele A



ClinVar
Risk rs2001030(G;G)
Alt rs2001030(G;G)
Reference rs2001030(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene
CLNDBN not specified
Reversed 0
HGVS NC_012920.1:m.1438A\x3d; NC_012920.1:m.1438A>G
CLNSRC
CLNACC RCV000154311.1, RCV000035045.2,