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rs397508165

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508165(A;A)
Make rs397508165(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117542034
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508165
ebirs397508165
HLIrs397508165
Exacrs397508165
Varsomers397508165
Maprs397508165
PheGenIrs397508165
hapmaprs397508165
1000 genomesrs397508165
hgdprs397508165
ensemblrs397508165
gopubmedrs397508165
geneviewrs397508165
scholarrs397508165
googlers397508165
pharmgkbrs397508165
gwascentralrs397508165
openSNPrs397508165
23andMers397508165
23andMe allrs397508165
SNP Nexus

SNPshotrs397508165
SNPdbers397508165
MSV3drs397508165
GWAS Ctlgrs397508165
Max Magnitude0
ClinVar
Risk rs397508165(A,T;A,T)
Alt rs397508165(A,T;A,T)
Reference rs397508165(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117182088G>A; NC_000007.13:g.117182088G>T
CLNSRC ClinVar
CLNACC RCV000046243.2, RCV000046244.2,