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rs104893958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893958(C;G)
Make rs104893958(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position1610823
GeneFOXC1
is asnp
is mentioned by
dbSNPrs104893958
ebirs104893958
HLIrs104893958
Exacrs104893958
Varsomers104893958
Maprs104893958
PheGenIrs104893958
hapmaprs104893958
1000 genomesrs104893958
hgdprs104893958
ensemblrs104893958
gopubmedrs104893958
geneviewrs104893958
scholarrs104893958
googlers104893958
pharmgkbrs104893958
gwascentralrs104893958
openSNPrs104893958
23andMers104893958
23andMe allrs104893958
SNP Nexus

SNPshotrs104893958
SNPdbers104893958
MSV3drs104893958
GWAS Ctlgrs104893958
Max Magnitude0
OMIM601090
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893958(A,G,T;A,G,T)
Alt rs104893958(A,G,T;A,G,T)
Reference rs104893958(C;C)
Significance Pathogenic
Disease Axenfeld anomaly
Variation info
Gene FOXC1
CLNDBN Axenfeld anomaly
Reversed 0
HGVS NC_000006.11:g.1611058C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008969.2,