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

rs587776947

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776947(-;-)
Make rs587776947(-;C)
ReferenceGRCh38 38.1/142
Chromosome1
Position113114434
GeneLRIG2
is asnp
is mentioned by
dbSNPrs587776947
ebirs587776947
HLIrs587776947
Exacrs587776947
Varsomers587776947
Maprs587776947
PheGenIrs587776947
hapmaprs587776947
1000 genomesrs587776947
hgdprs587776947
ensemblrs587776947
gopubmedrs587776947
geneviewrs587776947
scholarrs587776947
googlers587776947
pharmgkbrs587776947
gwascentralrs587776947
openSNPrs587776947
23andMers587776947
23andMe allrs587776947
SNP Nexus

SNPshotrs587776947
SNPdbers587776947
MSV3drs587776947
GWAS Ctlgrs587776947
Max Magnitude0
ClinVar
Risk rs587776947(;)
Alt rs587776947(;)
Reference rs587776947(C;C)
Significance Pathogenic
Disease Urofacial syndrome 2
Variation info
Gene LRIG2
CLNDBN Urofacial syndrome 2
Reversed 0
HGVS NC_000001.10:g.113657056delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000033226.5,