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rs587776507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCTGGCTGGCCTGT;CCTGGCTGGCCTGT) 0 common in clinvar
Make rs587776507(-;-)
Make rs587776507(-;TGGCCTGTCCTGGC)
Make rs587776507(TGGCCTGTCCTGGC;TGGCCTGTCCTGGC)
ReferenceGRCh38 38.1/142
Chromosome1
Position159205725
GeneACKR1
is asnp
is mentioned by
dbSNPrs587776507
dbSNP (old)rs587776507
ClinGenrs587776507
ebirs587776507
HLIrs587776507
Exacrs587776507
Varsomers587776507
Maprs587776507
PheGenIrs587776507
Biobankrs587776507
1000 genomesrs587776507
hgdprs587776507
ensemblrs587776507
gopubmedrs587776507
geneviewrs587776507
scholarrs587776507
googlers587776507
pharmgkbrs587776507
gwascentralrs587776507
openSNPrs587776507
23andMers587776507
23andMe allrs587776507
SNP Nexus

SNPshotrs587776507
SNPdbers587776507
MSV3drs587776507
GWAS Ctlgrs587776507
Max Magnitude0
ClinVar
Risk rs587776507(-;-)
Alt rs587776507(-;-)
Reference Rs587776507(CCTGGCTGGCCTGT;CCTGGCTGGCCTGT)
Significance Pathogenic
Disease DUFFY BLOOD GROUP SYSTEM
Variation info
Gene ACKR1
CLNDBN DUFFY BLOOD GROUP SYSTEM, FY(a-b-) PHENOTYPE
Reversed 0
HGVS NC_000001.10:g.159175515_159175528delTGGCCTGTCCTGGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000000010.3,