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rs397508654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508654(-;-)
Make rs397508654(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664700
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508654
ebirs397508654
HLIrs397508654
Exacrs397508654
Varsomers397508654
Maprs397508654
PheGenIrs397508654
hapmaprs397508654
1000 genomesrs397508654
hgdprs397508654
ensemblrs397508654
gopubmedrs397508654
geneviewrs397508654
scholarrs397508654
googlers397508654
pharmgkbrs397508654
gwascentralrs397508654
openSNPrs397508654
23andMers397508654
23andMe allrs397508654
SNP Nexus

SNPshotrs397508654
SNPdbers397508654
MSV3drs397508654
GWAS Ctlgrs397508654
Max Magnitude0
ClinVar
Risk rs397508654(;)
Alt rs397508654(;)
Reference rs397508654(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304754delT
CLNSRC ClinVar
CLNACC RCV000047049.2,