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rs121908773

From SNPedia

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


Make rs121908773(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117536609
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908773
ebirs121908773
HLIrs121908773
Exacrs121908773
Varsomers121908773
Maprs121908773
PheGenIrs121908773
hapmaprs121908773
1000 genomesrs121908773
hgdprs121908773
ensemblrs121908773
gopubmedrs121908773
geneviewrs121908773
scholarrs121908773
googlers121908773
pharmgkbrs121908773
gwascentralrs121908773
openSNPrs121908773
23andMers121908773
23andMe allrs121908773
SNP Nexus

SNPshotrs121908773
SNPdbers121908773
MSV3drs121908773
GWAS Ctlgrs121908773
Max Magnitude3
OMIM602421
Desc
Variant0101
Relatedalso
ClinVar
Risk rs121908773(;)
Alt rs121908773(;)
Reference rs121908773(AT;AT)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176663_117176664delAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007627.3,