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 3:41214354 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3198101

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2 sample genotypes.

Variant displays