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

rs398123009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123009(C;T)
Make rs398123009(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position66211206
GenePACS1
is asnp
is mentioned by
dbSNPrs398123009
ebirs398123009
HLIrs398123009
Exacrs398123009
Varsomers398123009
Maprs398123009
PheGenIrs398123009
hapmaprs398123009
1000 genomesrs398123009
hgdprs398123009
ensemblrs398123009
gopubmedrs398123009
geneviewrs398123009
scholarrs398123009
googlers398123009
pharmgkbrs398123009
gwascentralrs398123009
openSNPrs398123009
23andMers398123009
23andMe allrs398123009
SNP Nexus

SNPshotrs398123009
SNPdbers398123009
MSV3drs398123009
GWAS Ctlgrs398123009
Max Magnitude0
ClinVar
Risk rs398123009(T;T)
Alt rs398123009(T;T)
Reference rs398123009(C;C)
Significance Other
Disease Schuurs-hoeijmakers syndrome Multiple congenital anomalies Inborn genetic diseases
Variation info
Gene PACS1
CLNDBN Schuurs-hoeijmakers syndrome Multiple congenital anomalies Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.65978677C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032781.5, RCV000190758.1, RCV000210719.1,