Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP


Chromosome 5: between 148082984 and 148082985 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs375112446, rs200103553

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 5 sample genotypes.

Variant displays