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rs730882054

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCGGCGGCGGC;GCGGCGGCGGC) 0 common in clinvar
Make rs730882054(-;-)
Make rs730882054(-;CGGCGGCGCGG)
Make rs730882054(CGGCGGCGCGG;CGGCGGCGCGG)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position1611579
GeneFOXC1
is asnp
is mentioned by
dbSNPrs730882054
dbSNP (old)rs730882054
ClinGenrs730882054
ebirs730882054
HLIrs730882054
Exacrs730882054
Gnomadrs730882054
Varsomers730882054
Maprs730882054
PheGenIrs730882054
Biobankrs730882054
1000 genomesrs730882054
hgdprs730882054
ensemblrs730882054
gopubmedrs730882054
geneviewrs730882054
scholarrs730882054
googlers730882054
pharmgkbrs730882054
gwascentralrs730882054
openSNPrs730882054
23andMers730882054
23andMe allrs730882054
SNP Nexus

SNPshotrs730882054
SNPdbers730882054
MSV3drs730882054
GWAS Ctlgrs730882054
Max Magnitude0
ClinVar
Risk rs730882054(-;-)
Alt rs730882054(-;-)
Reference Rs730882054(GCGGCGGCGGC;GCGGCGGCGGC)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.1611814_1611824delCGGCGGCGCGG
CLNSRC
CLNACC RCV000162085.1,