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rs878853122

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853122(-;-)
Make rs878853122(-;G)
Make rs878853122(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position72225019
GeneINPPL1
is asnp
is mentioned by
dbSNPrs878853122
ebirs878853122
HLIrs878853122
Exacrs878853122
Varsomers878853122
Maprs878853122
PheGenIrs878853122
hapmaprs878853122
1000 genomesrs878853122
hgdprs878853122
ensemblrs878853122
gopubmedrs878853122
geneviewrs878853122
scholarrs878853122
googlers878853122
pharmgkbrs878853122
gwascentralrs878853122
openSNPrs878853122
23andMers878853122
23andMe allrs878853122
SNP Nexus

SNPshotrs878853122
SNPdbers878853122
MSV3drs878853122
GWAS Ctlgrs878853122
Max Magnitude0
ClinVar
Risk rs878853122(G;G)
Alt rs878853122(G;G)
Reference rs878853122(;)
Significance Pathogenic
Disease Opsismodysplasia
Variation info
Gene INPPL1
CLNDBN Opsismodysplasia
Reversed 0
HGVS NC_000011.9:g.71936063dupG
CLNSRC
CLNACC RCV000224773.1,