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rs587777527

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777527(A;A)
Make rs587777527(A;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position27254247
GeneRPL21, SNORA27, SNORD102
is asnp
is mentioned by
dbSNPrs587777527
ebirs587777527
HLIrs587777527
Exacrs587777527
Varsomers587777527
Maprs587777527
PheGenIrs587777527
hapmaprs587777527
1000 genomesrs587777527
hgdprs587777527
ensemblrs587777527
gopubmedrs587777527
geneviewrs587777527
scholarrs587777527
googlers587777527
pharmgkbrs587777527
gwascentralrs587777527
openSNPrs587777527
23andMers587777527
23andMe allrs587777527
SNP Nexus

SNPshotrs587777527
SNPdbers587777527
MSV3drs587777527
GWAS Ctlgrs587777527
Max Magnitude0
ClinVar
Risk rs587777527(A;A)
Alt rs587777527(A;A)
Reference rs587777527(G;G)
Significance Pathogenic
Disease Hypotrichosis 12
Variation info
Gene SNORA27 RPL21 SNORD102
CLNDBN Hypotrichosis 12
Reversed 0
HGVS NC_000013.10:g.27828384G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128579.2,