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rs201978662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201978662(A;A)
Make rs201978662(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592004
GeneCFTR
is asnp
is mentioned by
dbSNPrs201978662
ebirs201978662
HLIrs201978662
Exacrs201978662
Varsomers201978662
Maprs201978662
PheGenIrs201978662
hapmaprs201978662
1000 genomesrs201978662
hgdprs201978662
ensemblrs201978662
gopubmedrs201978662
geneviewrs201978662
scholarrs201978662
googlers201978662
pharmgkbrs201978662
gwascentralrs201978662
openSNPrs201978662
23andMers201978662
23andMe allrs201978662
SNP Nexus

SNPshotrs201978662
SNPdbers201978662
MSV3drs201978662
GWAS Ctlgrs201978662
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs201978662(A;A)
Alt rs201978662(A;A)
Reference rs201978662(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232058G>A
CLNSRC ClinVar
CLNACC RCV000046491.2,