Rs104894802

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894802(G;G)
Make rs104894802(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position68829885
GeneEFNB1
is asnp
is mentioned by
dbSNPrs104894802
Exacrs104894802
PheGenIrs104894802
nextbiors104894802
hapmaprs104894802
1000 genomesrs104894802
hgdprs104894802
ensemblrs104894802
gopubmedrs104894802
geneviewrs104894802
scholarrs104894802
googlers104894802
pharmgkbrs104894802
gwascentralrs104894802
openSNPrs104894802
23andMers104894802
23andMe allrs104894802
SNP Nexus

SNPshotrs104894802
SNPdbers104894802
MSV3drs104894802
Max Magnitude0
OMIM300035
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894802(G;G)
Alt rs104894802(G;G)
Reference rs104894802(T;T)
Significance Pathogenic
Disease Craniofrontonasal dysplasia
Variation info
Gene EFNB1
CLNDBN Craniofrontonasal dysplasia
Reversed 0
HGVS NC_000023.10:g.68049728T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012479.15,