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rs137852831

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852831(C;T)
Make rs137852831(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position41661923
GeneANK1, MIR486-1
is asnp
is mentioned by
dbSNPrs137852831
dbSNP (old)rs137852831
ClinGenrs137852831
ebirs137852831
HLIrs137852831
Exacrs137852831
Gnomadrs137852831
Varsomers137852831
Maprs137852831
PheGenIrs137852831
Biobankrs137852831
1000 genomesrs137852831
hgdprs137852831
ensemblrs137852831
gopubmedrs137852831
geneviewrs137852831
scholarrs137852831
googlers137852831
pharmgkbrs137852831
gwascentralrs137852831
openSNPrs137852831
23andMers137852831
23andMe allrs137852831
SNP Nexus

SNPshotrs137852831
SNPdbers137852831
MSV3drs137852831
GWAS Ctlgrs137852831
Max Magnitude0
OMIM612641
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852831(T;T)
Alt rs137852831(T;T)
Reference Rs137852831(C;C)
Significance Pathogenic
Disease Spherocytosis type 1
Variation info
Gene ANK1 MIR486-1
CLNDBN Spherocytosis type 1
Reversed 1
HGVS NC_000008.10:g.41519441G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000539.4,