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rs387906265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs387906265(-;-)
Make rs387906265(-;GA)
ReferenceGRCh38 38.1/141
Chromosome1
Position42830989
GeneERMAP
is asnp
is mentioned by
dbSNPrs387906265
ebirs387906265
HLIrs387906265
Exacrs387906265
Varsomers387906265
Maprs387906265
PheGenIrs387906265
hapmaprs387906265
1000 genomesrs387906265
hgdprs387906265
ensemblrs387906265
gopubmedrs387906265
geneviewrs387906265
scholarrs387906265
googlers387906265
pharmgkbrs387906265
gwascentralrs387906265
openSNPrs387906265
23andMers387906265
23andMe allrs387906265
SNP Nexus

SNPshotrs387906265
SNPdbers387906265
MSV3drs387906265
GWAS Ctlgrs387906265
Max Magnitude0
ClinVar
Risk rs387906265(;)
Alt rs387906265(;)
Reference rs387906265(GA;GA)
Significance Pathogenic
Disease SCIANNA BLOOD GROUP SYSTEM
Variation info
Gene ERMAP
CLNDBN SCIANNA BLOOD GROUP SYSTEM, SC:-1,-2
Reversed 0
HGVS NC_000001.10:g.43296660_43296661delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000001992.2,