Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906380

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;A) 3 cystic fibrosis carrier
Make rs387906380(-;-)
Make rs387906380(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117536664
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906380
ebirs387906380
HLIrs387906380
Exacrs387906380
Varsomers387906380
Maprs387906380
PheGenIrs387906380
hapmaprs387906380
1000 genomesrs387906380
hgdprs387906380
ensemblrs387906380
gopubmedrs387906380
geneviewrs387906380
scholarrs387906380
googlers387906380
pharmgkbrs387906380
gwascentralrs387906380
openSNPrs387906380
23andMers387906380
23andMe allrs387906380
SNP Nexus

SNPshotrs387906380
SNPdbers387906380
MSV3drs387906380
GWAS Ctlgrs387906380
Max Magnitude3
ClinVar
Risk rs387906380(A;A)
Alt rs387906380(A;A)
Reference rs387906380(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176718dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007658.3,