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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

rs1459880498

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr20:14326571 (GRCh38.p14)
Alleles
C>G / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.000004 (1/250734, GnomAD_exome)
Clinical Significance
Reported in ClinVar
Gene : Consequence
FLRT3 : Missense Variant
MACROD2 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
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Genomic regions, transcripts, and products
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Software version is: 2.0.1.post820+afb47a3d