Original source

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

Alleles
-/A/AAAAAA
Location

Chromosome 5: between 150127833 and 150127834 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs369419494

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

About this variant

This variant overlaps 6 transcripts.

Variation displays