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rs727504118

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504118(A;T)
Make rs727504118(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position17796531
GeneRAI1
is asnp
is mentioned by
dbSNPrs727504118
ebirs727504118
HLIrs727504118
Exacrs727504118
Varsomers727504118
Maprs727504118
PheGenIrs727504118
hapmaprs727504118
1000 genomesrs727504118
hgdprs727504118
ensemblrs727504118
gopubmedrs727504118
geneviewrs727504118
scholarrs727504118
googlers727504118
pharmgkbrs727504118
gwascentralrs727504118
openSNPrs727504118
23andMers727504118
23andMe allrs727504118
SNP Nexus

SNPshotrs727504118
SNPdbers727504118
MSV3drs727504118
GWAS Ctlgrs727504118
Max Magnitude0
ClinVar
Risk rs727504118(T;T)
Alt rs727504118(T;T)
Reference rs727504118(A;A)
Significance Pathogenic
Disease Smith-Magenis syndrome
Variation info
Gene RAI1
CLNDBN Smith-Magenis syndrome
Reversed 0
HGVS NC_000017.10:g.17699845A>T
CLNSRC
CLNACC RCV000153804.3,