Original source

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


Chromosome 4: between 174519218 and 174519219 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 26 HGVS names - click the plus to show

About this variant

This variant overlaps 26 transcripts and has 1 individual genotype.

Variation displays