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rs121909603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909603(A;A)
Make rs121909603(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position207322542
GeneCD55, LOC100129101
is asnp
is mentioned by
dbSNPrs121909603
ebirs121909603
HLIrs121909603
Exacrs121909603
Varsomers121909603
Maprs121909603
PheGenIrs121909603
hapmaprs121909603
1000 genomesrs121909603
hgdprs121909603
ensemblrs121909603
gopubmedrs121909603
geneviewrs121909603
scholarrs121909603
googlers121909603
pharmgkbrs121909603
gwascentralrs121909603
openSNPrs121909603
23andMers121909603
23andMe allrs121909603
SNP Nexus

SNPshotrs121909603
SNPdbers121909603
MSV3drs121909603
GWAS Ctlgrs121909603
Max Magnitude0
OMIM125240
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909603(A;A)
Alt rs121909603(A;A)
Reference rs121909603(G;G)
Significance Other
Disease Cromer blood group system
Variation info
Gene CD55
CLNDBN Cromer blood group system
Reversed 0
HGVS NC_000001.10:g.207495887G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018367.28,