Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (C)
Location

Chromosome 7:76436949 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs4077654, rs1638142

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

About this variant

This variant overlaps 7 transcripts and has 2505 sample genotypes.

Variant displays