Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.23 (C)
Location

Chromosome 20:37097648 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

20:g.37097648C>T

About this variant

This variant overlaps 8 transcripts and has 2581 individual genotypes.

Variation displays