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rs672601359

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs672601359(-;GGCCGCACCCCCGCCTC)
Make rs672601359(GGCCGCACCCCCGCCTC;GGCCGCACCCCCGCCTC)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position138945863
GeneFOXL2, FOXL2NB, LINC01391
is asnp
is mentioned by
dbSNPrs672601359
dbSNP (old)rs672601359
ClinGenrs672601359
ebirs672601359
HLIrs672601359
Exacrs672601359
Gnomadrs672601359
Varsomers672601359
Maprs672601359
PheGenIrs672601359
Biobankrs672601359
1000 genomesrs672601359
hgdprs672601359
ensemblrs672601359
gopubmedrs672601359
geneviewrs672601359
scholarrs672601359
googlers672601359
pharmgkbrs672601359
gwascentralrs672601359
openSNPrs672601359
23andMers672601359
23andMe allrs672601359
SNP Nexus

SNPshotrs672601359
SNPdbers672601359
MSV3drs672601359
GWAS Ctlgrs672601359
Max Magnitude0
ClinVar
Risk rs672601359(GGCCGCACCCCCGCCTC;GGCCGCACCCCCGCCTC)
Alt rs672601359(GGCCGCACCCCCGCCTC;GGCCGCACCCCCGCCTC)
Reference Rs672601359(-;-)
Significance Pathogenic
Disease Blepharophimosis
Variation info
Gene FOXL2 FOXL2NB C3orf72 LINC01391
CLNDBN Blepharophimosis, ptosis, and epicanthus inversus
Reversed 1
HGVS NC_000003.11:g.138664706_138664722dup17
CLNSRC
CLNACC RCV000149462.2,