Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.07 (T)
Location

Chromosome 7:31009576 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

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

This variation has assays on 9 chips - click the plus to show

Variation displays