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rs397508177

From SNPedia

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Geno Mag Summary
(A;G) 3 carrier of a cystic fibrosis allele
(G;G) 0 common in clinvar


Make rs397508177(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position117542108
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508177
ebirs397508177
HLIrs397508177
Exacrs397508177
Varsomers397508177
Maprs397508177
PheGenIrs397508177
hapmaprs397508177
1000 genomesrs397508177
hgdprs397508177
ensemblrs397508177
gopubmedrs397508177
geneviewrs397508177
scholarrs397508177
googlers397508177
pharmgkbrs397508177
gwascentralrs397508177
openSNPrs397508177
23andMers397508177
23andMe allrs397508177
SNP Nexus

SNPshotrs397508177
SNPdbers397508177
MSV3drs397508177
GWAS Ctlgrs397508177
Max Magnitude3
ClinVar
Risk rs397508177(A,C;A,C)
Alt rs397508177(A,C;A,C)
Reference rs397508177(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117182162G>A; NC_000007.13:g.117182162G>C
CLNSRC
CLNACC RCV000046259.2, RCV000046260.2,