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 14:90395012 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.90395012C>G

About this variant

This variant overlaps 13 transcripts and has 2504 individual genotypes.

Variation displays