Original source

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

Alleles
C/-|Ancestral: C|MAF: < 0.01 (C)
Location

Chromosome 14:92095499 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 50 HGVS names - Show

About this variant

This variant overlaps 51 transcripts and has 2507 sample genotypes.

Variant displays