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 14:102080475 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59380420, rs34399705

HGVS name

14:g.102080475C>G

About this variant

This variant overlaps 8 transcripts and has 2709 individual genotypes.

Variation displays