Original source

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

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

Chromosome 2:46384693 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3198334

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2505 individual genotypes.

Variation displays