Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.04 (G)
Location

Chromosome 7:139962165 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

This variation has 21 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 3615 individual genotypes.

Variation displays