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rs397508820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508820(A;A)
Make rs397508820(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540189
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508820
ebirs397508820
HLIrs397508820
Exacrs397508820
Varsomers397508820
Maprs397508820
PheGenIrs397508820
hapmaprs397508820
1000 genomesrs397508820
hgdprs397508820
ensemblrs397508820
gopubmedrs397508820
geneviewrs397508820
scholarrs397508820
googlers397508820
pharmgkbrs397508820
gwascentralrs397508820
openSNPrs397508820
23andMers397508820
23andMe allrs397508820
SNP Nexus

SNPshotrs397508820
SNPdbers397508820
MSV3drs397508820
GWAS Ctlgrs397508820
Max Magnitude0
ClinVar
Risk rs397508820(A;A)
Alt rs397508820(A;A)
Reference rs397508820(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180243T>A
CLNSRC ClinVar
CLNACC RCV000047297.2,