Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S
Location

Chromosome 12:6356399 (forward strand)|View in location tab

Most severe consequence
 
Splice region variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 262 sample genotypes.

Variant displays