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rs397508206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs397508206(-;-)
Make rs397508206(-;CA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559504
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508206
ebirs397508206
HLIrs397508206
Exacrs397508206
Varsomers397508206
Maprs397508206
PheGenIrs397508206
hapmaprs397508206
1000 genomesrs397508206
hgdprs397508206
ensemblrs397508206
gopubmedrs397508206
geneviewrs397508206
scholarrs397508206
googlers397508206
pharmgkbrs397508206
gwascentralrs397508206
openSNPrs397508206
23andMers397508206
23andMe allrs397508206
SNP Nexus

SNPshotrs397508206
SNPdbers397508206
MSV3drs397508206
GWAS Ctlgrs397508206
Max Magnitude0
ClinVar
Risk rs397508206(;)
Alt rs397508206(;)
Reference rs397508206(CA;CA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199558_117199559delCA
CLNSRC ClinVar
CLNACC RCV000046301.2,