Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.41 (A)
Location

Chromosome 7:93910178 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57376703, rs10330758

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2777 individual genotypes.

Variation displays