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rs150539474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150539474(C;T)
Make rs150539474(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position8325956
GeneSLC45A1
is asnp
is mentioned by
dbSNPrs150539474
dbSNP (classic)rs150539474
ClinGenrs150539474
ebirs150539474
HLIrs150539474
Exacrs150539474
Gnomadrs150539474
Varsomers150539474
LitVarrs150539474
Maprs150539474
PheGenIrs150539474
Biobankrs150539474
1000 genomesrs150539474
hgdprs150539474
ensemblrs150539474
geneviewrs150539474
scholarrs150539474
googlers150539474
pharmgkbrs150539474
gwascentralrs150539474
openSNPrs150539474
23andMers150539474
23andMe allrs150539474
SNPshotrs150539474
SNPdbers150539474
MSV3drs150539474
GWAS Ctlgrs150539474
Max Magnitude0
ClinVar
Risk rs150539474(T;T)
Alt rs150539474(T;T)
Reference Rs150539474(C;C)
Significance Pathogenic
Disease INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES
Variation info
Gene SLC45A1
CLNDBN INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES
Reversed 0
HGVS NC_000001.10:g.8386016C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000492063.1,