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rs137852830

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852830(A;A)
Make rs137852830(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position41668498
GeneANK1
is asnp
is mentioned by
dbSNPrs137852830
ebirs137852830
HLIrs137852830
Exacrs137852830
Varsomers137852830
Maprs137852830
PheGenIrs137852830
hapmaprs137852830
1000 genomesrs137852830
hgdprs137852830
ensemblrs137852830
gopubmedrs137852830
geneviewrs137852830
scholarrs137852830
googlers137852830
pharmgkbrs137852830
gwascentralrs137852830
openSNPrs137852830
23andMers137852830
23andMe allrs137852830
SNP Nexus

SNPshotrs137852830
SNPdbers137852830
MSV3drs137852830
GWAS Ctlgrs137852830
Max Magnitude0
OMIM612641
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852830(A;A)
Alt rs137852830(A;A)
Reference rs137852830(G;G)
Significance Pathogenic
Disease Spherocytosis type 1
Variation info
Gene ANK1
CLNDBN Spherocytosis type 1
Reversed 1
HGVS NC_000008.10:g.41526016C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000538.3,