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rs587776945

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776945(-;-)
Make rs587776945(-;A)
ReferenceGRCh38 38.1/142
Chromosome1
Position113100268
GeneLRIG2
is asnp
is mentioned by
dbSNPrs587776945
ebirs587776945
HLIrs587776945
Exacrs587776945
Varsomers587776945
Maprs587776945
PheGenIrs587776945
hapmaprs587776945
1000 genomesrs587776945
hgdprs587776945
ensemblrs587776945
gopubmedrs587776945
geneviewrs587776945
scholarrs587776945
googlers587776945
pharmgkbrs587776945
gwascentralrs587776945
openSNPrs587776945
23andMers587776945
23andMe allrs587776945
SNP Nexus

SNPshotrs587776945
SNPdbers587776945
MSV3drs587776945
GWAS Ctlgrs587776945
Max Magnitude0
ClinVar
Risk rs587776945(;)
Alt rs587776945(;)
Reference rs587776945(A;A)
Significance Pathogenic
Disease Urofacial syndrome 2
Variation info
Gene LRIG2
CLNDBN Urofacial syndrome 2
Reversed 0
HGVS NC_000001.10:g.113642890delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000033224.5,