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rs145483167

From SNPedia

Orientationplus
Stabilizedplus
Make rs145483167(A;A)
Make rs145483167(A;G)
Make rs145483167(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position117479930
GeneCFTR
is asnp
is mentioned by
dbSNPrs145483167
dbSNP (old)rs145483167
ClinGenrs145483167
ebirs145483167
HLIrs145483167
Exacrs145483167
Gnomadrs145483167
Varsomers145483167
LitVarrs145483167
Maprs145483167
PheGenIrs145483167
Biobankrs145483167
1000 genomesrs145483167
hgdprs145483167
ensemblrs145483167
gopubmedrs145483167
geneviewrs145483167
scholarrs145483167
googlers145483167
pharmgkbrs145483167
gwascentralrs145483167
openSNPrs145483167
23andMers145483167
23andMe allrs145483167
SNPshotrs145483167
SNPdbers145483167
MSV3drs145483167
GWAS Ctlgrs145483167
Max Magnitude

[PMID 27569544OA-icon.png] A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. This SNP maps to a position listed in Table S6 as a non-coding variant that their biocurators felt was convincingly associated with a Mendelian disease.