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rs397508710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508710(-;-)
Make rs397508710(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117480136
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508710
ClinGenrs397508710
ebirs397508710
HLIrs397508710
Exacrs397508710
Varsomers397508710
Maprs397508710
PheGenIrs397508710
hapmaprs397508710
1000 genomesrs397508710
hgdprs397508710
ensemblrs397508710
gopubmedrs397508710
geneviewrs397508710
scholarrs397508710
googlers397508710
pharmgkbrs397508710
gwascentralrs397508710
openSNPrs397508710
23andMers397508710
23andMe allrs397508710
SNP Nexus

SNPshotrs397508710
SNPdbers397508710
MSV3drs397508710
GWAS Ctlgrs397508710
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397508710(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117120190delA
CLNSRC ClinVar
CLNACC RCV000047126.2,