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

rs397508768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508768(A;A)
Make rs397508768(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535274
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508768
ebirs397508768
HLIrs397508768
Exacrs397508768
Varsomers397508768
Maprs397508768
PheGenIrs397508768
hapmaprs397508768
1000 genomesrs397508768
hgdprs397508768
ensemblrs397508768
gopubmedrs397508768
geneviewrs397508768
scholarrs397508768
googlers397508768
pharmgkbrs397508768
gwascentralrs397508768
openSNPrs397508768
23andMers397508768
23andMe allrs397508768
SNP Nexus

SNPshotrs397508768
SNPdbers397508768
MSV3drs397508768
GWAS Ctlgrs397508768
Max Magnitude0
ClinVar
Risk rs397508768(A;A)
Alt rs397508768(A;A)
Reference rs397508768(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175328G>A
CLNSRC ClinVar
CLNACC RCV000047217.2,