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rs121908785

From SNPedia

Cystic Fibrosis related
Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;AT) 3 carrier of a cystic fibrosis allele
Make rs121908785(-;-)
Make rs121908785(AT;AT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117542052
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908785
ebirs121908785
HLIrs121908785
Exacrs121908785
Varsomers121908785
Maprs121908785
PheGenIrs121908785
hapmaprs121908785
1000 genomesrs121908785
hgdprs121908785
ensemblrs121908785
gopubmedrs121908785
geneviewrs121908785
scholarrs121908785
googlers121908785
pharmgkbrs121908785
gwascentralrs121908785
openSNPrs121908785
23andMers121908785
23andMe allrs121908785
SNP Nexus

SNPshotrs121908785
SNPdbers121908785
MSV3drs121908785
GWAS Ctlgrs121908785
Max Magnitude3

Cystic fibrosis; c.1153_1154insAT, p.Asn386Ilefs

named i5011146 by 23andMe


ClinVar
Risk rs121908785(AT;AT)
Alt rs121908785(AT;AT)
Reference rs121908785(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117182105_117182106dupAT
CLNSRC CFTR2
CLNACC RCV000046247.3,