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rs61732609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61732609(C;C)
Make rs61732609(C;T)
Make rs61732609(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position42627674
GeneCYB5R3
is asnp
is mentioned by
dbSNPrs61732609
ebirs61732609
HLIrs61732609
Exacrs61732609
Varsomers61732609
Maprs61732609
PheGenIrs61732609
hapmaprs61732609
1000 genomesrs61732609
hgdprs61732609
ensemblrs61732609
gopubmedrs61732609
geneviewrs61732609
scholarrs61732609
googlers61732609
pharmgkbrs61732609
gwascentralrs61732609
openSNPrs61732609
23andMers61732609
23andMe allrs61732609
SNP Nexus

SNPshotrs61732609
SNPdbers61732609
MSV3drs61732609
GWAS Ctlgrs61732609
Max Magnitude0
OMIM613213
Desc
Variant0015
Relatedalso
ClinVar
Risk rs61732609(A;A)
Alt rs61732609(A;A)
Reference rs61732609(G;G)
Significance Pathogenic
Disease Methemoglobinemia type 2
Variation info
Gene CYB5R3
CLNDBN Methemoglobinemia type 2
Reversed 0
HGVS NC_000022.10:g.43023680G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000272.3,