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rs387906366

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;CTATG) 3 cystic fibrosis carrier
Make rs387906366(-;-)
Make rs387906366(CTATG;CTATG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611629
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906366
ebirs387906366
HLIrs387906366
Exacrs387906366
Varsomers387906366
Maprs387906366
PheGenIrs387906366
hapmaprs387906366
1000 genomesrs387906366
hgdprs387906366
ensemblrs387906366
gopubmedrs387906366
geneviewrs387906366
scholarrs387906366
googlers387906366
pharmgkbrs387906366
gwascentralrs387906366
openSNPrs387906366
23andMers387906366
23andMe allrs387906366
SNP Nexus

SNPshotrs387906366
SNPdbers387906366
MSV3drs387906366
GWAS Ctlgrs387906366
Max Magnitude3
ClinVar
Risk rs387906366(CTATG;CTATG)
Alt rs387906366(CTATG;CTATG)
Reference rs387906366(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251679_117251683dupCTATG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007581.3,