Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: < 0.01 (G)
Location

Chromosome 12:48772276 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2774 sample genotypes.

Variant displays