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rs397508411

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGTTGTGC;GGTTGTGC) 0 common in clinvar
Make rs397508411(-;-)
Make rs397508411(-;GGTTGTGC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117602840
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508411
ebirs397508411
HLIrs397508411
Exacrs397508411
Varsomers397508411
Maprs397508411
PheGenIrs397508411
hapmaprs397508411
1000 genomesrs397508411
hgdprs397508411
ensemblrs397508411
gopubmedrs397508411
geneviewrs397508411
scholarrs397508411
googlers397508411
pharmgkbrs397508411
gwascentralrs397508411
openSNPrs397508411
23andMers397508411
23andMe allrs397508411
SNP Nexus

SNPshotrs397508411
SNPdbers397508411
MSV3drs397508411
GWAS Ctlgrs397508411
Max Magnitude0
ClinVar
Risk rs397508411(;)
Alt rs397508411(;)
Reference rs397508411(GGTTGTGC;GGTTGTGC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117242894_117242901delGGTTGTGC
CLNSRC ClinVar
CLNACC RCV000046641.2,