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rs121908158

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908158(C;C)
Make rs121908158(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position14954009
GeneDCLRE1C, MEIG1
is asnp
is mentioned by
dbSNPrs121908158
ebirs121908158
HLIrs121908158
Exacrs121908158
Varsomers121908158
Maprs121908158
PheGenIrs121908158
hapmaprs121908158
1000 genomesrs121908158
hgdprs121908158
ensemblrs121908158
gopubmedrs121908158
geneviewrs121908158
scholarrs121908158
googlers121908158
pharmgkbrs121908158
gwascentralrs121908158
openSNPrs121908158
23andMers121908158
23andMe allrs121908158
SNP Nexus

SNPshotrs121908158
SNPdbers121908158
MSV3drs121908158
GWAS Ctlgrs121908158
Max Magnitude0
OMIM605988
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121908158(C;C)
Alt rs121908158(C;C)
Reference rs121908158(T;T)
Significance Pathogenic
Disease Histiocytic medullary reticulosis
Variation info
Gene MEIG1 DCLRE1C
CLNDBN Histiocytic medullary reticulosis
Reversed 1
HGVS NC_000010.10:g.14996008A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004941.2,