Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508777(A;A)
Make rs397508777(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535321
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508777
ebirs397508777
HLIrs397508777
Exacrs397508777
Varsomers397508777
Maprs397508777
PheGenIrs397508777
hapmaprs397508777
1000 genomesrs397508777
hgdprs397508777
ensemblrs397508777
gopubmedrs397508777
geneviewrs397508777
scholarrs397508777
googlers397508777
pharmgkbrs397508777
gwascentralrs397508777
openSNPrs397508777
23andMers397508777
23andMe allrs397508777
SNP Nexus

SNPshotrs397508777
SNPdbers397508777
MSV3drs397508777
GWAS Ctlgrs397508777
Max Magnitude0
ClinVar
Risk rs397508777(A;A)
Alt rs397508777(A;A)
Reference rs397508777(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175375T>A
CLNSRC ClinVar
CLNACC RCV000047229.2,