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rs387906519

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCTC;CCTC) 0 common in clinvar
Make rs387906519(CCTC;GA)
Make rs387906519(GA;GA)
ReferenceGRCh38 38.1/141
Chromosome6
Position49636656
GeneRHAG
is asnp
is mentioned by
dbSNPrs387906519
ebirs387906519
HLIrs387906519
Exacrs387906519
Varsomers387906519
Maprs387906519
PheGenIrs387906519
hapmaprs387906519
1000 genomesrs387906519
hgdprs387906519
ensemblrs387906519
gopubmedrs387906519
geneviewrs387906519
scholarrs387906519
googlers387906519
pharmgkbrs387906519
gwascentralrs387906519
openSNPrs387906519
23andMers387906519
23andMe allrs387906519
SNP Nexus

SNPshotrs387906519
SNPdbers387906519
MSV3drs387906519
GWAS Ctlgrs387906519
Max Magnitude0
ClinVar
Risk rs387906519(GA;GA)
Alt rs387906519(GA;GA)
Reference rs387906519(CCTC;CCTC)
Significance Pathogenic
Disease Rh-null hemolytic anemia
Variation info
Gene RHAG
CLNDBN Rh-null hemolytic anemia, regulator type
Reversed 1
HGVS NC_000006.11:g.49604369_49604372delGAGGinsTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000013932.25,