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rs869320717

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320717(-;-)
Make rs869320717(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position44309772
GeneALX4
is asnp
is mentioned by
dbSNPrs869320717
ebirs869320717
HLIrs869320717
Exacrs869320717
Varsomers869320717
Maprs869320717
PheGenIrs869320717
hapmaprs869320717
1000 genomesrs869320717
hgdprs869320717
ensemblrs869320717
gopubmedrs869320717
geneviewrs869320717
scholarrs869320717
googlers869320717
pharmgkbrs869320717
gwascentralrs869320717
openSNPrs869320717
23andMers869320717
23andMe allrs869320717
SNP Nexus

SNPshotrs869320717
SNPdbers869320717
MSV3drs869320717
GWAS Ctlgrs869320717
Max Magnitude0
ClinVar
Risk rs869320717(;)
Alt rs869320717(;)
Reference rs869320717(G;G)
Significance Pathogenic
Disease Frontonasal dysplasia 2
Variation info
Gene ALX4
CLNDBN Frontonasal dysplasia 2
Reversed 1
HGVS NC_000011.9:g.44331322delC
CLNSRC
CLNACC RCV000210924.1,