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rs397508673

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508673(A;T)
Make rs397508673(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117480134
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508673
ebirs397508673
HLIrs397508673
Exacrs397508673
Varsomers397508673
Maprs397508673
PheGenIrs397508673
hapmaprs397508673
1000 genomesrs397508673
hgdprs397508673
ensemblrs397508673
gopubmedrs397508673
geneviewrs397508673
scholarrs397508673
googlers397508673
pharmgkbrs397508673
gwascentralrs397508673
openSNPrs397508673
23andMers397508673
23andMe allrs397508673
SNP Nexus

SNPshotrs397508673
SNPdbers397508673
MSV3drs397508673
GWAS Ctlgrs397508673
Max Magnitude0
ClinVar
Risk rs397508673(T;T)
Alt rs397508673(T;T)
Reference rs397508673(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117120188A>T
CLNSRC ClinVar
CLNACC RCV000047073.2,