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rs397508164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs397508164(-;-)
Make rs397508164(-;TA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117504311
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508164
ebirs397508164
HLIrs397508164
Exacrs397508164
Varsomers397508164
Maprs397508164
PheGenIrs397508164
hapmaprs397508164
1000 genomesrs397508164
hgdprs397508164
ensemblrs397508164
gopubmedrs397508164
geneviewrs397508164
scholarrs397508164
googlers397508164
pharmgkbrs397508164
gwascentralrs397508164
openSNPrs397508164
23andMers397508164
23andMe allrs397508164
SNP Nexus

SNPshotrs397508164
SNPdbers397508164
MSV3drs397508164
GWAS Ctlgrs397508164
Max Magnitude0
ClinVar
Risk rs397508164(;)
Alt rs397508164(;)
Reference rs397508164(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,