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rs397508414

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;A) 2 possibly a cystic fibrosis carrier, but maybe not
Make rs397508414(-;-)
Make rs397508414(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117602865
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508414
ebirs397508414
HLIrs397508414
Exacrs397508414
Varsomers397508414
Maprs397508414
PheGenIrs397508414
hapmaprs397508414
1000 genomesrs397508414
hgdprs397508414
ensemblrs397508414
gopubmedrs397508414
geneviewrs397508414
scholarrs397508414
googlers397508414
pharmgkbrs397508414
gwascentralrs397508414
openSNPrs397508414
23andMers397508414
23andMe allrs397508414
SNP Nexus

SNPshotrs397508414
SNPdbers397508414
MSV3drs397508414
GWAS Ctlgrs397508414
Max Magnitude2
ClinVar
Risk rs397508414(A;A)
Alt rs397508414(A;A)
Reference rs397508414(;)
Significance Pathogenic
Disease Cystic fibrosis not provided
Variation info
Gene CFTR
CLNDBN Cystic fibrosis not provided
Reversed 0
HGVS NC_000007.13:g.117242919_117242920insA
CLNSRC HGMD
CLNACC RCV000046646.3, RCV000078986.3,