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rs587776925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776925(A;A)
Make rs587776925(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position203863714
GeneSNRPE
is asnp
is mentioned by
dbSNPrs587776925
ebirs587776925
HLIrs587776925
Exacrs587776925
Varsomers587776925
Maprs587776925
PheGenIrs587776925
hapmaprs587776925
1000 genomesrs587776925
hgdprs587776925
ensemblrs587776925
gopubmedrs587776925
geneviewrs587776925
scholarrs587776925
googlers587776925
pharmgkbrs587776925
gwascentralrs587776925
openSNPrs587776925
23andMers587776925
23andMe allrs587776925
SNP Nexus

SNPshotrs587776925
SNPdbers587776925
MSV3drs587776925
GWAS Ctlgrs587776925
Max Magnitude0
ClinVar
Risk rs587776925(A;A)
Alt rs587776925(A;A)
Reference rs587776925(G;G)
Significance Pathogenic
Disease Hypotrichosis 11
Variation info
Gene SNRPE
CLNDBN Hypotrichosis 11
Reversed 0
HGVS NC_000001.10:g.203832842G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032702.27,