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rs886041901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCTGT;TCTGT) 0 common in clinvar
Chromosome16
Position67628521
GeneCTCF
is asnp
is mentioned by
dbSNPrs886041901
dbSNP (classic)rs886041901
ClinGenrs886041901
ebirs886041901
HLIrs886041901
Exacrs886041901
Gnomadrs886041901
Varsomers886041901
LitVarrs886041901
Maprs886041901
PheGenIrs886041901
Biobankrs886041901
1000 genomesrs886041901
hgdprs886041901
ensemblrs886041901
geneviewrs886041901
scholarrs886041901
googlers886041901
pharmgkbrs886041901
gwascentralrs886041901
openSNPrs886041901
23andMers886041901
SNPshotrs886041901
SNPdbers886041901
MSV3drs886041901
GWAS Ctlgrs886041901
Max Magnitude0
ClinVar
Risk rs886041901(-;-)
Alt rs886041901(-;-)
Reference Rs886041901(TCTGT;TCTGT)
Significance Pathogenic
Disease not provided
Variation info
Gene CTCF
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.67662424_67662428delGTTCT
CLNSRC
CLNACC RCV000284751.1,