Original source

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

Alleles
ATTCCAG/-|MAF: < 0.01 (ATTCCAG)
Location

Chromosome 16:30747150-30747156 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs149647812

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2512 sample genotypes.

Variant displays