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rs527236033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236033(A;A)
Make rs527236033(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position17795221
GeneRAI1
is asnp
is mentioned by
dbSNPrs527236033
ebirs527236033
HLIrs527236033
Exacrs527236033
Varsomers527236033
Maprs527236033
PheGenIrs527236033
hapmaprs527236033
1000 genomesrs527236033
hgdprs527236033
ensemblrs527236033
gopubmedrs527236033
geneviewrs527236033
scholarrs527236033
googlers527236033
pharmgkbrs527236033
gwascentralrs527236033
openSNPrs527236033
23andMers527236033
23andMe allrs527236033
SNP Nexus

SNPshotrs527236033
SNPdbers527236033
MSV3drs527236033
GWAS Ctlgrs527236033
Max Magnitude0
ClinVar
Risk rs527236033(A;A)
Alt rs527236033(A;A)
Reference rs527236033(G;G)
Significance Pathogenic
Disease Smith-Magenis syndrome
Variation info
Gene RAI1
CLNDBN Smith-Magenis syndrome
Reversed 0
HGVS NC_000017.10:g.17698535G>A
CLNSRC ClinVar
CLNACC RCV000132731.1,