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rs28939377

From SNPedia

Merged intors119478058
Orientationplus
Stabilizedplus
Make rs28939377(C;C)
Make rs28939377(C;T)
Make rs28939377(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position102923789
GeneAMN
is asnp
is mentioned by
dbSNPrs28939377
ebirs28939377
HLIrs28939377
Exacrs28939377
Varsomers28939377
Maprs28939377
PheGenIrs28939377
hapmaprs28939377
1000 genomesrs28939377
hgdprs28939377
ensemblrs28939377
gopubmedrs28939377
geneviewrs28939377
scholarrs28939377
googlers28939377
pharmgkbrs28939377
gwascentralrs28939377
openSNPrs28939377
23andMers28939377
23andMe allrs28939377
SNP Nexus

SNPshotrs28939377
SNPdbers28939377
MSV3drs28939377
GWAS Ctlgrs28939377
StatusMerged into rs119478058
Max Magnitude
OMIM605799
DescMEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
Variant0002
Relatedalso