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rs387906870

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs387906870(-;-)
Make rs387906870(-;TT)
ReferenceGRCh38 38.1/141
Chromosome4
Position88118158
GeneABCG2
is asnp
is mentioned by
dbSNPrs387906870
ebirs387906870
HLIrs387906870
Exacrs387906870
Varsomers387906870
Maprs387906870
PheGenIrs387906870
hapmaprs387906870
1000 genomesrs387906870
hgdprs387906870
ensemblrs387906870
gopubmedrs387906870
geneviewrs387906870
scholarrs387906870
googlers387906870
pharmgkbrs387906870
gwascentralrs387906870
openSNPrs387906870
23andMers387906870
23andMe allrs387906870
SNP Nexus

SNPshotrs387906870
SNPdbers387906870
MSV3drs387906870
GWAS Ctlgrs387906870
Max Magnitude0
ClinVar
Risk rs387906870(;)
Alt rs387906870(;)
Reference rs387906870(TT;TT)
Significance Other
Disease Blood group
Variation info
Gene ABCG2
CLNDBN Blood group, Junior system
Reversed 1
HGVS NC_000004.11:g.89039310_89039311delAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000023340.4,