Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.24 (C)
Location

Chromosome 15:78453365 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57445303

This variation has 8 HGVS names - click the plus to show

15:g.78453365C>T
ENST00000560454.1:n.523-9557C>T
ENST00000560840.4:c.-65-9557C>T
ENST00000258886.11:c.107-9557C>T
ENST00000559215.4:c.107-11886C>T
ENST00000560440.4:c.107-9557C>T
ENST00000558525.4:c.102-9557C>T
ENST00000558570.4:c.107-9557C>T

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2365 individual genotypes and is mentioned in 5 citations.

Variation displays