Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.21 (G)

Chromosome 1:7975211 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs574572, rs707480

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 11 transcripts and has 1107 individual genotypes.

Variation displays