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rs118204087

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs118204087(A;A)
Make rs118204087(A;G)
ReferenceGRCh37 37.1/132
Chromosome1
Position155270062
GenePKLR
is asnp
is mentioned by
dbSNPrs118204087
ebirs118204087
HLIrs118204087
Exacrs118204087
Varsomers118204087
Maprs118204087
PheGenIrs118204087
hapmaprs118204087
1000 genomesrs118204087
hgdprs118204087
ensemblrs118204087
gopubmedrs118204087
geneviewrs118204087
scholarrs118204087
googlers118204087
pharmgkbrs118204087
gwascentralrs118204087
openSNPrs118204087
23andMers118204087
23andMe allrs118204087
SNP Nexus

SNPshotrs118204087
SNPdbers118204087
MSV3drs118204087
GWAS Ctlgrs118204087
Max Magnitude0
OMIM609712
Desc
Variant0008
Relatedalso
ClinVar
Risk rs118204087(A,T;A,T)
Alt rs118204087(A,T;A,T)
Reference rs118204087(G;G)
Significance Pathogenic
Disease Adenosine triphosphate
Variation info
Gene PKLR
CLNDBN Adenosine triphosphate, elevated, of erythrocytes
Reversed 1
HGVS NC_000001.10:g.155270062C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001576.2,