Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776924

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776924(A;G)
Make rs587776924(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position203861660
GeneSNRPE
is asnp
is mentioned by
dbSNPrs587776924
ebirs587776924
HLIrs587776924
Exacrs587776924
Varsomers587776924
Maprs587776924
PheGenIrs587776924
hapmaprs587776924
1000 genomesrs587776924
hgdprs587776924
ensemblrs587776924
gopubmedrs587776924
geneviewrs587776924
scholarrs587776924
googlers587776924
pharmgkbrs587776924
gwascentralrs587776924
openSNPrs587776924
23andMers587776924
23andMe allrs587776924
SNP Nexus

SNPshotrs587776924
SNPdbers587776924
MSV3drs587776924
GWAS Ctlgrs587776924
Max Magnitude0
ClinVar
Risk rs587776924(G;G)
Alt rs587776924(G;G)
Reference rs587776924(A;A)
Significance Pathogenic
Disease Hypotrichosis 11
Variation info
Gene SNRPE
CLNDBN Hypotrichosis 11
Reversed 0
HGVS NC_000001.10:g.203830788A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000032701.28,