Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 10:74103822 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB VCL_2025G_A_091410

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

About this variant

This variant overlaps 9 transcripts, has 2504 individual genotypes and is associated with 2 phenotypes.

Variation displays