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rs878853135

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853135(-;-)
Make rs878853135(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position10671578
GenePIEZO2
is asnp
is mentioned by
dbSNPrs878853135
ebirs878853135
HLIrs878853135
Exacrs878853135
Varsomers878853135
Maprs878853135
PheGenIrs878853135
hapmaprs878853135
1000 genomesrs878853135
hgdprs878853135
ensemblrs878853135
gopubmedrs878853135
geneviewrs878853135
scholarrs878853135
googlers878853135
pharmgkbrs878853135
gwascentralrs878853135
openSNPrs878853135
23andMers878853135
23andMe allrs878853135
SNP Nexus

SNPshotrs878853135
SNPdbers878853135
MSV3drs878853135
GWAS Ctlgrs878853135
Max Magnitude0
ClinVar
Risk rs878853135(;)
Alt rs878853135(;)
Reference rs878853135(A;A)
Significance Pathogenic
Disease Oculomelic amyoplasia
Variation info
Gene PIEZO2
CLNDBN Oculomelic amyoplasia
Reversed 1
HGVS NC_000018.9:g.10671575delT
CLNSRC
CLNACC RCV000223972.1,