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rs199474668

From SNPedia

Merged intors193303018
Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199474668(A;A)
Make rs199474668(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position3242
is asnp
is mentioned by
dbSNPrs199474668
ebirs199474668
HLIrs199474668
Exacrs199474668
Varsomers199474668
Maprs199474668
PheGenIrs199474668
hapmaprs199474668
1000 genomesrs199474668
hgdprs199474668
ensemblrs199474668
gopubmedrs199474668
geneviewrs199474668
scholarrs199474668
googlers199474668
pharmgkbrs199474668
gwascentralrs199474668
openSNPrs199474668
23andMers199474668
23andMe allrs199474668
SNP Nexus

SNPshotrs199474668
SNPdbers199474668
MSV3drs199474668
GWAS Ctlgrs199474668
StatusMerged into rs193303018
Max Magnitude0
ClinVar
Risk rs199474668(A;A)
Alt rs199474668(A;A)
Reference rs199474668(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 RCV000010223.4,