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rs397508204

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGTGATTATG;GGTGATTATG) 0 common in clinvar
(GTGATTATGG;GTGATTATGG) 0 common in clinvar
Make rs397508204(-;-)
Make rs397508204(-;GTGATTATGG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559479
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508204
dbSNP (classic)rs397508204
ClinGenrs397508204
ebirs397508204
HLIrs397508204
Exacrs397508204
Gnomadrs397508204
Varsomers397508204
LitVarrs397508204
Maprs397508204
PheGenIrs397508204
Biobankrs397508204
1000 genomesrs397508204
hgdprs397508204
ensemblrs397508204
geneviewrs397508204
scholarrs397508204
googlers397508204
pharmgkbrs397508204
gwascentralrs397508204
openSNPrs397508204
23andMers397508204
SNPshotrs397508204
SNPdbers397508204
MSV3drs397508204
GWAS Ctlgrs397508204
Max Magnitude0
ClinVar
Risk rs397508204(-;-)
Alt rs397508204(-;-)
Reference Rs397508204(GGTGATTATG;GGTGATTATG)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199533_117199542delGTGATTATGG
CLNSRC ClinVar
CLNACC RCV000046299.2,