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rs397508162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs397508162(-;-)
Make rs397508162(-;AT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117504310
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508162
ebirs397508162
HLIrs397508162
Exacrs397508162
Varsomers397508162
Maprs397508162
PheGenIrs397508162
hapmaprs397508162
1000 genomesrs397508162
hgdprs397508162
ensemblrs397508162
gopubmedrs397508162
geneviewrs397508162
scholarrs397508162
googlers397508162
pharmgkbrs397508162
gwascentralrs397508162
openSNPrs397508162
23andMers397508162
23andMe allrs397508162
SNP Nexus

SNPshotrs397508162
SNPdbers397508162
MSV3drs397508162
GWAS Ctlgrs397508162
Max Magnitude0
ClinVar
Risk rs397508162(;)
Alt rs397508162(;)
Reference rs397508162(AT;AT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117144365_117144366delTA
CLNSRC ClinVar
CLNACC RCV000046242.4,