Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.25 (C)
Location

Chromosome 6:143939848 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59481575, rs17524513

HGVS name

6:g.143939848C>G

About this variant

This variant overlaps 19 transcripts and has 2510 individual genotypes.

Variation displays