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rs387906869

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs387906869(-;-)
Make rs387906869(-;AC)
ReferenceGRCh38 38.1/141
Chromosome4
Position88113385
GeneABCG2
is asnp
is mentioned by
dbSNPrs387906869
ebirs387906869
HLIrs387906869
Exacrs387906869
Varsomers387906869
Maprs387906869
PheGenIrs387906869
hapmaprs387906869
1000 genomesrs387906869
hgdprs387906869
ensemblrs387906869
gopubmedrs387906869
geneviewrs387906869
scholarrs387906869
googlers387906869
pharmgkbrs387906869
gwascentralrs387906869
openSNPrs387906869
23andMers387906869
23andMe allrs387906869
SNP Nexus

SNPshotrs387906869
SNPdbers387906869
MSV3drs387906869
GWAS Ctlgrs387906869
Max Magnitude0
ClinVar
Risk rs387906869(;)
Alt rs387906869(;)
Reference rs387906869(AC;AC)
Significance Other
Disease Blood group
Variation info
Gene ABCG2
CLNDBN Blood group, Junior system
Reversed 1
HGVS NC_000004.11:g.89034537_89034538delGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000023334.4,