Have questions? Visit https://www.reddit.com/r/SNPedia

rs200190472

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200190472(C;T)
Make rs200190472(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position88118214
GeneABCG2
is asnp
is mentioned by
dbSNPrs200190472
ebirs200190472
HLIrs200190472
Exacrs200190472
Varsomers200190472
Maprs200190472
PheGenIrs200190472
hapmaprs200190472
1000 genomesrs200190472
hgdprs200190472
ensemblrs200190472
gopubmedrs200190472
geneviewrs200190472
scholarrs200190472
googlers200190472
pharmgkbrs200190472
gwascentralrs200190472
openSNPrs200190472
23andMers200190472
23andMe allrs200190472
SNP Nexus

SNPshotrs200190472
SNPdbers200190472
MSV3drs200190472
GWAS Ctlgrs200190472
Max Magnitude0
ClinVar
Risk rs200190472(T;T)
Alt rs200190472(T;T)
Reference rs200190472(C;C)
Significance Other
Disease Blood group
Variation info
Gene ABCG2
CLNDBN Blood group, Junior system
Reversed 1
HGVS NC_000004.11:g.89039366G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023333.4,