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rs28929497

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs28929497(G;G)
Make rs28929497(G;T)
ReferenceGRCh37 37.1/131
Chromosome1
Position196716367
GeneCFH
is asnp
is mentioned by
dbSNPrs28929497
dbSNP (classic)rs28929497
ClinGenrs28929497
ebirs28929497
HLIrs28929497
Exacrs28929497
Gnomadrs28929497
Varsomers28929497
LitVarrs28929497
Maprs28929497
PheGenIrs28929497
Biobankrs28929497
1000 genomesrs28929497
hgdprs28929497
ensemblrs28929497
geneviewrs28929497
scholarrs28929497
googlers28929497
pharmgkbrs28929497
gwascentralrs28929497
openSNPrs28929497
23andMers28929497
SNPshotrs28929497
SNPdbers28929497
MSV3drs28929497
GWAS Ctlgrs28929497
StatusDeleted
Max Magnitude0
OMIM134370
DescHEMOLYTIC UREMIC SYNDROME, ATYPICAL
Variant0007
Relatedalso
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