Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]


Chromosome 13: between 23193527 and 23193528 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs142518344

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 1 individual genotype.

Variation displays