Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.44 (T)
Location

Chromosome 13:35657351 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56674030

This variation has 7 HGVS names - click the plus to show

13:g.35657351T>G
ENST00000379922.3:c.1033+1602T>G
ENST00000400445.6:c.8299+1602T>G
ENST00000310336.7:c.8302+1602T>G
ENST00000629018.1:c.8299+1602T>G
ENST00000537702.4:c.1678+1602T>G
ENST00000379939.5:c.8290+1602T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_Human1M-duo

About this variant

This variant overlaps 6 transcripts, has 2225 individual genotypes and is mentioned in 1 citation.

Variation displays