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rs587776946

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776946(C;T)
Make rs587776946(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position113114471
GeneLRIG2
is asnp
is mentioned by
dbSNPrs587776946
ebirs587776946
HLIrs587776946
Exacrs587776946
Varsomers587776946
Maprs587776946
PheGenIrs587776946
hapmaprs587776946
1000 genomesrs587776946
hgdprs587776946
ensemblrs587776946
gopubmedrs587776946
geneviewrs587776946
scholarrs587776946
googlers587776946
pharmgkbrs587776946
gwascentralrs587776946
openSNPrs587776946
23andMers587776946
23andMe allrs587776946
SNP Nexus

SNPshotrs587776946
SNPdbers587776946
MSV3drs587776946
GWAS Ctlgrs587776946
Max Magnitude0
ClinVar
Risk rs587776946(T;T)
Alt rs587776946(T;T)
Reference rs587776946(C;C)
Significance Pathogenic
Disease Urofacial syndrome 2
Variation info
Gene LRIG2
CLNDBN Urofacial syndrome 2
Reversed 0
HGVS NC_000001.10:g.113657093C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033225.5,