Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 7:94639305 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 265 sample genotypes.

Variant displays