Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.33 (T)
Location

Chromosome 7:147491593 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs10373812, rs57823747

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

7:g.147491593G>T
ENST00000361727.5:c.1777+5552G>T

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0

Variation displays