Original source

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

T/-/TT | Ancestral: T

Chromosome 1:26748628 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs75641038

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 1 individual genotype.

Variation displays