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rs587777616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777616(A;A)
Make rs587777616(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position57659895
GeneCLP1
is asnp
is mentioned by
dbSNPrs587777616
ebirs587777616
HLIrs587777616
Exacrs587777616
Varsomers587777616
Maprs587777616
PheGenIrs587777616
hapmaprs587777616
1000 genomesrs587777616
hgdprs587777616
ensemblrs587777616
gopubmedrs587777616
geneviewrs587777616
scholarrs587777616
googlers587777616
pharmgkbrs587777616
gwascentralrs587777616
openSNPrs587777616
23andMers587777616
23andMe allrs587777616
SNP Nexus

SNPshotrs587777616
SNPdbers587777616
MSV3drs587777616
GWAS Ctlgrs587777616
Max Magnitude0
ClinVar
Risk rs587777616(A;A)
Alt rs587777616(A;A)
Reference rs587777616(G;G)
Significance Other
Disease Pontocerebellar hypoplasia
Variation info
Gene CLP1
CLNDBN Pontocerebellar hypoplasia, type 10
Reversed 0
HGVS NC_000011.9:g.57427367G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000133463.3,