{{Rsnum
|rsid=387907363
|Chromosome=22
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=SNAP29
|position=20881101
|Gene_s=SNAP29
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CA
|CHROM=22
|CLNACC=RCV000043503.3
|CLNALLE=1
|CLNDBN=Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1836033:609528:66631
|CLNHGVS=NC_000022.10:g.21235389_21235390insA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604202.0002
|Disease=Cerebral dysgenesis
|FwdALT=A
|REF=C
|RSPOS=21235388
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387907363
|GENEINFO=SNAP29:9342
|GENE_ID=9342
|GENE_NAME=SNAP29
}}