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rs104893987

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893987(A;A)
Make rs104893987(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position49612504
GeneRHAG
is asnp
is mentioned by
dbSNPrs104893987
ebirs104893987
HLIrs104893987
Exacrs104893987
Varsomers104893987
Maprs104893987
PheGenIrs104893987
hapmaprs104893987
1000 genomesrs104893987
hgdprs104893987
ensemblrs104893987
gopubmedrs104893987
geneviewrs104893987
scholarrs104893987
googlers104893987
pharmgkbrs104893987
gwascentralrs104893987
openSNPrs104893987
23andMers104893987
23andMe allrs104893987
SNP Nexus

SNPshotrs104893987
SNPdbers104893987
MSV3drs104893987
GWAS Ctlgrs104893987
Max Magnitude0
OMIM180297
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104893987(A;A)
Alt rs104893987(A;A)
Reference rs104893987(G;G)
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.49580217C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013940.24,