Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2505 sample genotypes.

Variant displays