Have questions? Visit https://www.reddit.com/r/SNPedia

rs869025335

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025335(C;T)
Make rs869025335(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position204406262
GenePPP1R15B
is asnp
is mentioned by
dbSNPrs869025335
ebirs869025335
HLIrs869025335
Exacrs869025335
Varsomers869025335
Maprs869025335
PheGenIrs869025335
hapmaprs869025335
1000 genomesrs869025335
hgdprs869025335
ensemblrs869025335
gopubmedrs869025335
geneviewrs869025335
scholarrs869025335
googlers869025335
pharmgkbrs869025335
gwascentralrs869025335
openSNPrs869025335
23andMers869025335
23andMe allrs869025335
SNP Nexus

SNPshotrs869025335
SNPdbers869025335
MSV3drs869025335
GWAS Ctlgrs869025335
Max Magnitude0
ClinVar
Risk rs869025335(T;T)
Alt rs869025335(T;T)
Reference rs869025335(C;C)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene PPP1R15B
CLNDBN Microcephaly, short stature, and impaired glucose metabolism 2
Reversed 1
HGVS NC_000001.10:g.204375390G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000207486.1,