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rs121908775

From SNPedia

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


Make rs121908775(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559548
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908775
ebirs121908775
HLIrs121908775
Exacrs121908775
Varsomers121908775
Maprs121908775
PheGenIrs121908775
hapmaprs121908775
1000 genomesrs121908775
hgdprs121908775
ensemblrs121908775
gopubmedrs121908775
geneviewrs121908775
scholarrs121908775
googlers121908775
pharmgkbrs121908775
gwascentralrs121908775
openSNPrs121908775
23andMers121908775
23andMe allrs121908775
SNP Nexus

SNPshotrs121908775
SNPdbers121908775
MSV3drs121908775
GWAS Ctlgrs121908775
Max Magnitude3
OMIM602421
Desc
Variant0115
Relatedalso
ClinVar
Risk rs121908775(;)
Alt rs121908775(;)
Reference rs121908775(CA;CA)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199602_117199603delCA
CLNSRC CFTR2 OMIM Allelic Variant
CLNACC RCV000007640.3,