Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.13 (G)
Location

Chromosome 7:30975950 (forward strand) | View in location tab

Most severe consequence

 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

Evidence status

Synonyms

Archive dbSNP rs59653211, rs52835078

This variation has 9 HGVS names - click the plus to show

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

Variation displays