Original source

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

C/T | Ambiguity code: Y

Chromosome 17:47150871 (forward strand) | View in location tab

Most severe consequence

This variation has 2 synonyms - click the plus to show

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2 individual genotypes.

Variation displays