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rs397508775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508775(A;A)
Make rs397508775(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535315
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508775
ebirs397508775
HLIrs397508775
Exacrs397508775
Varsomers397508775
Maprs397508775
PheGenIrs397508775
hapmaprs397508775
1000 genomesrs397508775
hgdprs397508775
ensemblrs397508775
gopubmedrs397508775
geneviewrs397508775
scholarrs397508775
googlers397508775
pharmgkbrs397508775
gwascentralrs397508775
openSNPrs397508775
23andMers397508775
23andMe allrs397508775
SNP Nexus

SNPshotrs397508775
SNPdbers397508775
MSV3drs397508775
GWAS Ctlgrs397508775
Max Magnitude0
ClinVar
Risk rs397508775(A;A)
Alt rs397508775(A;A)
Reference rs397508775(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175369G>A
CLNSRC ClinVar
CLNACC RCV000047227.2,