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

rs397508767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508767(-;-)
Make rs397508767(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535269
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508767
ebirs397508767
HLIrs397508767
Exacrs397508767
Varsomers397508767
Maprs397508767
PheGenIrs397508767
hapmaprs397508767
1000 genomesrs397508767
hgdprs397508767
ensemblrs397508767
gopubmedrs397508767
geneviewrs397508767
scholarrs397508767
googlers397508767
pharmgkbrs397508767
gwascentralrs397508767
openSNPrs397508767
23andMers397508767
23andMe allrs397508767
SNP Nexus

SNPshotrs397508767
SNPdbers397508767
MSV3drs397508767
GWAS Ctlgrs397508767
Max Magnitude0
ClinVar
Risk rs397508767(;)
Alt rs397508767(;)
Reference rs397508767(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175323delG
CLNSRC ClinVar
CLNACC RCV000047216.2,