Original source

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

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

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