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rs397508229

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508229(A;G)
Make rs397508229(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117578327
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508229
ebirs397508229
HLIrs397508229
Exacrs397508229
Varsomers397508229
Maprs397508229
PheGenIrs397508229
hapmaprs397508229
1000 genomesrs397508229
hgdprs397508229
ensemblrs397508229
gopubmedrs397508229
geneviewrs397508229
scholarrs397508229
googlers397508229
pharmgkbrs397508229
gwascentralrs397508229
openSNPrs397508229
23andMers397508229
23andMe allrs397508229
SNP Nexus

SNPshotrs397508229
SNPdbers397508229
MSV3drs397508229
GWAS Ctlgrs397508229
Max Magnitude0
ClinVar
Risk rs397508229(G;G)
Alt rs397508229(G;G)
Reference rs397508229(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117218381A>G
CLNSRC ClinVar
CLNACC RCV000046345.2,