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rs397508196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508196(-;-)
Make rs397508196(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548804
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508196
ebirs397508196
HLIrs397508196
Exacrs397508196
Varsomers397508196
Maprs397508196
PheGenIrs397508196
hapmaprs397508196
1000 genomesrs397508196
hgdprs397508196
ensemblrs397508196
gopubmedrs397508196
geneviewrs397508196
scholarrs397508196
googlers397508196
pharmgkbrs397508196
gwascentralrs397508196
openSNPrs397508196
23andMers397508196
23andMe allrs397508196
SNP Nexus

SNPshotrs397508196
SNPdbers397508196
MSV3drs397508196
GWAS Ctlgrs397508196
Max Magnitude0
ClinVar
Risk rs397508196(;)
Alt rs397508196(;)
Reference rs397508196(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188858delG
CLNSRC ClinVar
CLNACC RCV000046285.2,