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

rs121965010

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121965010(C;T)
Make rs121965010(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position42623867
GeneCYB5R3
is asnp
is mentioned by
dbSNPrs121965010
dbSNP (classic)rs121965010
ClinGenrs121965010
ebirs121965010
HLIrs121965010
Exacrs121965010
Gnomadrs121965010
Varsomers121965010
LitVarrs121965010
Maprs121965010
PheGenIrs121965010
Biobankrs121965010
1000 genomesrs121965010
hgdprs121965010
ensemblrs121965010
geneviewrs121965010
scholarrs121965010
googlers121965010
pharmgkbrs121965010
gwascentralrs121965010
openSNPrs121965010
23andMers121965010
SNPshotrs121965010
SNPdbers121965010
MSV3drs121965010
GWAS Ctlgrs121965010
Max Magnitude0
OMIM613213
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121965010(T;T)
Alt rs121965010(T;T)
Reference Rs121965010(C;C)
Significance Pathogenic
Disease Methemoglobinemia type 2
Variation info
Gene CYB5R3
CLNDBN Methemoglobinemia type 2
Reversed 1
HGVS NC_000022.10:g.43019873G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000264.3,