Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.47 (G)
Location

Chromosome 7:31095890 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs10386990, rs56702131

This variation has 7 HGVS names - click the plus to show

7:g.31095890C>G
ENST00000409363.2:c.983+3155C>G
ENST00000409489.2:c.1130+140C>G
ENST00000614107.1:c.1046+3155C>G
ENST00000304166.5:c.1046+3155C>G
ENST00000396211.3:c.1046+3155C>G
ENST00000436116.1:c.279+140C>G

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays