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rs794727365

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727365(A;A)
Make rs794727365(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position78364055
GeneFRAS1
is asnp
is mentioned by
dbSNPrs794727365
ebirs794727365
HLIrs794727365
Exacrs794727365
Varsomers794727365
Maprs794727365
PheGenIrs794727365
hapmaprs794727365
1000 genomesrs794727365
hgdprs794727365
ensemblrs794727365
gopubmedrs794727365
geneviewrs794727365
scholarrs794727365
googlers794727365
pharmgkbrs794727365
gwascentralrs794727365
openSNPrs794727365
23andMers794727365
23andMe allrs794727365
SNP Nexus

SNPshotrs794727365
SNPdbers794727365
MSV3drs794727365
GWAS Ctlgrs794727365
Max Magnitude0
ClinVar
Risk rs794727365(A;A)
Alt rs794727365(A;A)
Reference rs794727365(G;G)
Significance Pathogenic
Disease Cryptophthalmos syndrome not provided
Variation info
Gene FRAS1
CLNDBN Cryptophthalmos syndrome not provided
Reversed 0
HGVS NC_000004.11:g.79285209G>A
CLNSRC
CLNACC RCV000176329.1, RCV000224135.1,