Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.28 (G)
Location

Chromosome 15:77671545 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59418404

This variation has 10 HGVS names - click the plus to show

15:g.77671545A>G
ENST00000570216.4:c.-13+5544T>C
ENST00000559893.4:c.-13+5544T>C
ENST00000562933.4:c.-13+5544T>C
ENST00000563316.4:c.-13+5544T>C
ENST00000567726.4:c.-13+5544T>C
ENST00000561030.4:c.-13+5544T>C
ENST00000566711.4:c.-13+5544T>C
ENST00000561686.4:c.-13+19175T>C
ENST00000564472.4:c.-13+5544T>C

This variation has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2288 individual genotypes, is associated with 1 phenotype and is mentioned in 34 citations.

Variation displays