Original source

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

Alleles
-/TT | MAF: 0.44 (TT)
Location

Chromosome 10: between 62389439 and 62389440 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2510 individual genotypes.

Variation displays