Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B | MAF: < 0.01 (A)
Location

Chromosome 19:48987362 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_037958

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2771 individual genotypes.

Variation displays