Original source

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

Alleles
-/G | MAF: 0.19 (-)
Location

Chromosome 19: between 16485848 and 16485849 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs376552064

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2510 individual genotypes.

Variation displays