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rs137853206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853206(A;G)
Make rs137853206(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position33036828
GeneAK2
is asnp
is mentioned by
dbSNPrs137853206
ebirs137853206
HLIrs137853206
Exacrs137853206
Varsomers137853206
Maprs137853206
PheGenIrs137853206
hapmaprs137853206
1000 genomesrs137853206
hgdprs137853206
ensemblrs137853206
gopubmedrs137853206
geneviewrs137853206
scholarrs137853206
googlers137853206
pharmgkbrs137853206
gwascentralrs137853206
openSNPrs137853206
23andMers137853206
23andMe allrs137853206
SNP Nexus

SNPshotrs137853206
SNPdbers137853206
MSV3drs137853206
GWAS Ctlgrs137853206
Max Magnitude0
OMIM103020
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853206(G;G)
Alt rs137853206(G;G)
Reference rs137853206(A;A)
Significance Pathogenic
Disease Reticular dysgenesis
Variation info
Gene AK2
CLNDBN Reticular dysgenesis
Reversed 1
HGVS NC_000001.10:g.33502429T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019914.28,