Original source

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

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

Chromosome 9:35095410 (forward strand) | View in location tab

Most severe consequence
 
Missense variant

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 251 sample genotypes.

Variant displays