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rs121908159

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908159(C;G)
Make rs121908159(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position14953908
GeneDCLRE1C, MEIG1
is asnp
is mentioned by
dbSNPrs121908159
ebirs121908159
HLIrs121908159
Exacrs121908159
Varsomers121908159
Maprs121908159
PheGenIrs121908159
hapmaprs121908159
1000 genomesrs121908159
hgdprs121908159
ensemblrs121908159
gopubmedrs121908159
geneviewrs121908159
scholarrs121908159
googlers121908159
pharmgkbrs121908159
gwascentralrs121908159
openSNPrs121908159
23andMers121908159
23andMe allrs121908159
SNP Nexus

SNPshotrs121908159
SNPdbers121908159
MSV3drs121908159
GWAS Ctlgrs121908159
Max Magnitude0
OMIM605988
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121908159(G;G)
Alt rs121908159(G;G)
Reference rs121908159(C;C)
Significance Pathogenic
Disease Histiocytic medullary reticulosis
Variation info
Gene MEIG1 DCLRE1C
CLNDBN Histiocytic medullary reticulosis
Reversed 1
HGVS NC_000010.10:g.14995907G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004938.3,