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rs193303018

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193303018(A;A)
Make rs193303018(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeMT
Position3242
is asnp
is mentioned by
dbSNPrs193303018
ebirs193303018
HLIrs193303018
Exacrs193303018
Varsomers193303018
Maprs193303018
PheGenIrs193303018
hapmaprs193303018
1000 genomesrs193303018
hgdprs193303018
ensemblrs193303018
gopubmedrs193303018
geneviewrs193303018
scholarrs193303018
googlers193303018
pharmgkbrs193303018
gwascentralrs193303018
openSNPrs193303018
23andMers193303018
23andMe allrs193303018
SNP Nexus

SNPshotrs193303018
SNPdbers193303018
MSV3drs193303018
GWAS Ctlgrs193303018
Merged fromRs199474668
Max Magnitude0
ClinVar
Risk rs193303018(A;A)
Alt rs193303018(A;A)
Reference rs193303018(G;G)
Significance Pathogenic
Disease Myelodysplastic syndrome
Variation info
Gene
CLNDBN Myelodysplastic syndrome
Reversed 0
HGVS NC_012920.1:m.3242G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010223.5,