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rs587784275

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs587784275(-;-)
Make rs587784275(-;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2672733
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784275
ebirs587784275
HLIrs587784275
Exacrs587784275
Varsomers587784275
Maprs587784275
PheGenIrs587784275
hapmaprs587784275
1000 genomesrs587784275
hgdprs587784275
ensemblrs587784275
gopubmedrs587784275
geneviewrs587784275
scholarrs587784275
googlers587784275
pharmgkbrs587784275
gwascentralrs587784275
openSNPrs587784275
23andMers587784275
23andMe allrs587784275
SNP Nexus

SNPshotrs587784275
SNPdbers587784275
MSV3drs587784275
GWAS Ctlgrs587784275
Max Magnitude0
ClinVar
Risk rs587784275(;)
Alt rs587784275(;)
Reference rs587784275(TA;TA)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2576027_2576028delTA
CLNSRC
CLNACC RCV000147048.1,