Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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

rs1436272523

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr12:120765002-120765010 (GRCh38.p14)
Alleles
delTACTTCCAG
Variation Type
Deletion
Frequency
None
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SPPL3 : Inframe Deletion
Publications
0 citations
Genomic View
See rs on genome
None

Genomic regions, transcripts, and products
Top

Software version is: 2.0.1.post820+afb47a3d