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rs121908762

From SNPedia

Merged intors121908761
Orientationplus
Stabilizedplus
Make rs121908762(A;A)
Make rs121908762(A;C)
Make rs121908762(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611717
GeneCFTR
is asnp
is mentioned by
dbSNPrs121908762
ebirs121908762
HLIrs121908762
Exacrs121908762
Varsomers121908762
Maprs121908762
PheGenIrs121908762
hapmaprs121908762
1000 genomesrs121908762
hgdprs121908762
ensemblrs121908762
gopubmedrs121908762
geneviewrs121908762
scholarrs121908762
googlers121908762
pharmgkbrs121908762
gwascentralrs121908762
openSNPrs121908762
23andMers121908762
23andMe allrs121908762
SNP Nexus

SNPshotrs121908762
SNPdbers121908762
MSV3drs121908762
GWAS Ctlgrs121908762
StatusMerged into rs121908761
Max Magnitude
OMIM602421
Desc
Variant0106
Relatedalso


[PMID 15948195] Mutation spectrum in Jewish cystic fibrosis patients in Israel: implication to carrier screening.