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rs28939699

From SNPedia

Merged intors121434430
Orientationminus
Stabilizedminus
Make rs28939699(C;C)
Make rs28939699(C;T)
Make rs28939699(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position17041160
GeneCUBN
is asnp
is mentioned by
dbSNPrs28939699
ebirs28939699
HLIrs28939699
Exacrs28939699
Varsomers28939699
Maprs28939699
PheGenIrs28939699
hapmaprs28939699
1000 genomesrs28939699
hgdprs28939699
ensemblrs28939699
gopubmedrs28939699
geneviewrs28939699
scholarrs28939699
googlers28939699
pharmgkbrs28939699
gwascentralrs28939699
openSNPrs28939699
23andMers28939699
23andMe allrs28939699
SNP Nexus

SNPshotrs28939699
SNPdbers28939699
MSV3drs28939699
GWAS Ctlgrs28939699
StatusMerged into rs121434430
Max Magnitude
OMIM602997
DescMEGALOBLASTIC ANEMIA 1, FINNISH TYPE
Variant0001
Relatedalso