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rs104893957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893957(C;T)
Make rs104893957(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position1610837
GeneFOXC1
is asnp
is mentioned by
dbSNPrs104893957
ebirs104893957
HLIrs104893957
Exacrs104893957
Varsomers104893957
Maprs104893957
PheGenIrs104893957
hapmaprs104893957
1000 genomesrs104893957
hgdprs104893957
ensemblrs104893957
gopubmedrs104893957
geneviewrs104893957
scholarrs104893957
googlers104893957
pharmgkbrs104893957
gwascentralrs104893957
openSNPrs104893957
23andMers104893957
23andMe allrs104893957
SNP Nexus

SNPshotrs104893957
SNPdbers104893957
MSV3drs104893957
GWAS Ctlgrs104893957
Max Magnitude0
OMIM601090
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893957(T;T)
Alt rs104893957(T;T)
Reference rs104893957(C;C)
Significance Pathogenic
Disease Axenfeld-Rieger syndrome type 3
Variation info
Gene FOXC1
CLNDBN Axenfeld-Rieger syndrome type 3
Reversed 0
HGVS NC_000006.11:g.1611072C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008968.2,