Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.49 (T)

Chromosome 11:102592876 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs7949109

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2507 individual genotypes.

Variation displays