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rs183894680

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs183894680(C;T)
Make rs183894680(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position41797691
GeneANK1, LOC105379392
is asnp
is mentioned by
dbSNPrs183894680
ebirs183894680
HLIrs183894680
Exacrs183894680
Varsomers183894680
Maprs183894680
PheGenIrs183894680
hapmaprs183894680
1000 genomesrs183894680
hgdprs183894680
ensemblrs183894680
gopubmedrs183894680
geneviewrs183894680
scholarrs183894680
googlers183894680
pharmgkbrs183894680
gwascentralrs183894680
openSNPrs183894680
23andMers183894680
23andMe allrs183894680
SNP Nexus

SNPshotrs183894680
SNPdbers183894680
MSV3drs183894680
GWAS Ctlgrs183894680
Max Magnitude0
ClinVar
Risk rs183894680(T;T)
Alt rs183894680(T;T)
Reference rs183894680(C;C)
Significance Pathogenic
Disease Spherocytosis
Variation info
Gene ANK1
CLNDBN Spherocytosis, type 1, autosomal recessive
Reversed 0
HGVS NC_000008.10:g.41655209C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000541.4,