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rs773442562

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTG;TTG) 0 common in clinvar
Make rs773442562(-;-)
Make rs773442562(-;TTG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position92266452
GeneGLMN
is asnp
is mentioned by
dbSNPrs773442562
dbSNP (old)rs773442562
ClinGenrs773442562
ebirs773442562
HLIrs773442562
Exacrs773442562
Varsomers773442562
Maprs773442562
PheGenIrs773442562
Biobankrs773442562
1000 genomesrs773442562
hgdprs773442562
ensemblrs773442562
gopubmedrs773442562
geneviewrs773442562
scholarrs773442562
googlers773442562
pharmgkbrs773442562
gwascentralrs773442562
openSNPrs773442562
23andMers773442562
23andMe allrs773442562
SNP Nexus

SNPshotrs773442562
SNPdbers773442562
MSV3drs773442562
GWAS Ctlgrs773442562
Max Magnitude0
ClinVar
Risk rs773442562(-;-)
Alt rs773442562(-;-)
Reference Rs773442562(TTG;TTG)
Significance Pathogenic
Disease Glomuvenous malformations
Variation info
Gene GLMN
CLNDBN Glomuvenous malformations
Reversed 0
HGVS NC_000001.10:g.92732009_92732011delTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000008250.2,