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rs555387669

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs555387669(-;-)
Make rs555387669(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position32637143
GeneARHGAP11A
is asnp
is mentioned by
dbSNPrs555387669
ebirs555387669
HLIrs555387669
Exacrs555387669
Varsomers555387669
Maprs555387669
PheGenIrs555387669
hapmaprs555387669
1000 genomesrs555387669
hgdprs555387669
ensemblrs555387669
gopubmedrs555387669
geneviewrs555387669
scholarrs555387669
googlers555387669
pharmgkbrs555387669
gwascentralrs555387669
openSNPrs555387669
23andMers555387669
23andMe allrs555387669
SNP Nexus

SNPshotrs555387669
SNPdbers555387669
MSV3drs555387669
GWAS Ctlgrs555387669
Max Magnitude0
ClinVar
Risk rs555387669(;)
Alt rs555387669(;)
Reference rs555387669(AT;AT)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ARHGAP11A
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000015.9:g.32929344_32929345delAT
CLNSRC
CLNACC RCV000210601.1,