Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs2073868
- Species
- Homo sapiens
- Symbol
- rs2073868
- Category
- Variant
- Variant type
- SNP
- Overlaps
- POLDIP2
- Location
- 17:28348239
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- (GRCh38)17:28348239C>T
- HGVS.c name
- ENSEMBL:ENST00000540200.6:c.993-8G>A
- ENSEMBL:ENST00000618887.2:c.939-8G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:28346633...28357527 (10.89 kb)
- Assembly version
- Not Available
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