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rs397508661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508661(-;-)
Make rs397508661(-;GGGG)
Make rs397508661(GGGG;GGGG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664752
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508661
ebirs397508661
HLIrs397508661
Exacrs397508661
Varsomers397508661
Maprs397508661
PheGenIrs397508661
hapmaprs397508661
1000 genomesrs397508661
hgdprs397508661
ensemblrs397508661
gopubmedrs397508661
geneviewrs397508661
scholarrs397508661
googlers397508661
pharmgkbrs397508661
gwascentralrs397508661
openSNPrs397508661
23andMers397508661
23andMe allrs397508661
SNP Nexus

SNPshotrs397508661
SNPdbers397508661
MSV3drs397508661
GWAS Ctlgrs397508661
Max Magnitude0
ClinVar
Risk rs397508661(GGGG;GGGG)
Alt rs397508661(GGGG;GGGG)
Reference rs397508661(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304803_117304806dupGGGG
CLNSRC ClinVar
CLNACC RCV000047058.2,