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rs727502802

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs727502802(-;-)
Make rs727502802(-;A)
Make rs727502802(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position112756799
GeneCKAP2L
is asnp
is mentioned by
dbSNPrs727502802
ebirs727502802
HLIrs727502802
Exacrs727502802
Varsomers727502802
Maprs727502802
PheGenIrs727502802
hapmaprs727502802
1000 genomesrs727502802
hgdprs727502802
ensemblrs727502802
gopubmedrs727502802
geneviewrs727502802
scholarrs727502802
googlers727502802
pharmgkbrs727502802
gwascentralrs727502802
openSNPrs727502802
23andMers727502802
23andMe allrs727502802
SNP Nexus

SNPshotrs727502802
SNPdbers727502802
MSV3drs727502802
GWAS Ctlgrs727502802
Max Magnitude0
ClinVar
Risk rs727502802(A;A)
Alt rs727502802(A;A)
Reference rs727502802(;)
Significance Pathogenic
Disease Filippi syndrome
Variation info
Gene CKAP2L
CLNDBN Filippi syndrome
Reversed 1
HGVS NC_000002.11:g.113514377dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000149779.3,