Original source

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

Alleles
-/T
Location

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

Most severe consequence
Synonyms

Archive dbSNP rs375112446, rs200103553

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

About this variant

This variant overlaps 7 transcripts and has 5 individual genotypes.

Variation displays