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

rs387906365

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CT) 3 cystic fibrosis carrier
(CT;CT) 0 common in clinvar


Make rs387906365(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540323
GeneCFTR
is asnp
is mentioned by
dbSNPrs387906365
dbSNP (classic)rs387906365
ClinGenrs387906365
ebirs387906365
HLIrs387906365
Exacrs387906365
Gnomadrs387906365
Varsomers387906365
LitVarrs387906365
Maprs387906365
PheGenIrs387906365
Biobankrs387906365
1000 genomesrs387906365
hgdprs387906365
ensemblrs387906365
geneviewrs387906365
scholarrs387906365
googlers387906365
pharmgkbrs387906365
gwascentralrs387906365
openSNPrs387906365
23andMers387906365
SNPshotrs387906365
SNPdbers387906365
MSV3drs387906365
GWAS Ctlgrs387906365
Max Magnitude3
ClinVar
Risk rs387906365(-;-)
Alt rs387906365(-;-)
Reference Rs387906365(CT;CT)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180377_117180378delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007574.3,