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rs121908781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 3 carrier of a cystic fibrosis allele
(C;C) 0 common in clinvar


Make rs121908781(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610569
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908781
ebirs121908781
HLIrs121908781
Exacrs121908781
Varsomers121908781
Maprs121908781
PheGenIrs121908781
hapmaprs121908781
1000 genomesrs121908781
hgdprs121908781
ensemblrs121908781
gopubmedrs121908781
geneviewrs121908781
scholarrs121908781
googlers121908781
pharmgkbrs121908781
gwascentralrs121908781
openSNPrs121908781
23andMers121908781
23andMe allrs121908781
SNP Nexus

SNPshotrs121908781
SNPdbers121908781
MSV3drs121908781
GWAS Ctlgrs121908781
Max Magnitude3
ClinVar
Risk rs121908781(;)
Alt rs121908781(;)
Reference rs121908781(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250623delC
CLNSRC CFTR2
CLNACC RCV000046765.3,