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rs137853234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853234(C;C)
Make rs137853234(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position72060463
GeneHP
is asnp
is mentioned by
dbSNPrs137853234
ebirs137853234
HLIrs137853234
Exacrs137853234
Varsomers137853234
Maprs137853234
PheGenIrs137853234
hapmaprs137853234
1000 genomesrs137853234
hgdprs137853234
ensemblrs137853234
gopubmedrs137853234
geneviewrs137853234
scholarrs137853234
googlers137853234
pharmgkbrs137853234
gwascentralrs137853234
openSNPrs137853234
23andMers137853234
23andMe allrs137853234
SNP Nexus

SNPshotrs137853234
SNPdbers137853234
MSV3drs137853234
GWAS Ctlgrs137853234
Max Magnitude0
OMIM140100
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853234(C;C)
Alt rs137853234(C;C)
Reference rs137853234(T;T)
Significance Untested
Disease Anhaptoglobinemia
Variation info
Gene HP
CLNDBN Anhaptoglobinemia
Reversed 0
HGVS NC_000016.9:g.72094362T>C
CLNSRC OMIM Allelic Variant
CLNACC SCV000037521.1, SCV000037521.1,